Skip to main content

Ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate

ADVERTISEMENT
Identification
Molecular formula
C19H20N2O2S
CAS number
20358-87-6
IUPAC name
ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate
State
State

At room temperature, this compound is a solid. Given its complex structure, it is not particularly volatile and remains stable under standard ambient conditions.

Melting point (Celsius)
197.00
Melting point (Kelvin)
470.15
Boiling point (Celsius)
512.00
Boiling point (Kelvin)
785.15
General information
Molecular weight
328.43g/mol
Molar mass
328.4280g/mol
Density
1.3200g/cm3
Appearence

Ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate typically appears as a crystalline solid. The compound is a complex organic molecule and can have a white to off-white coloration depending on purity and specific conditions of crystallization.

Comment on solubility

Solubility of Ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate

The solubility of ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate (C19H20N2O2S) can be influenced by various factors, making it a compound of interest in solubility studies. Here are some key points to consider:

  • Polarity: Due to its thieno and pyridine rings, the compound might exhibit moderate polarity, affecting its solubility in polar and non-polar solvents.
  • Functional Groups: The presence of multiple functional groups, such as the carboxylate and amino groups, suggests possible interactions with water, potentially enhancing solubility in aqueous environments.
  • Environment: Solubility can vary significantly with pH. For instance, at higher pH levels, the carboxylate could become deprotonated, increasing the solubility in water.
  • Temperature Influence: Typically, an increase in temperature can improve solubility for many organic compounds; thus, this may also apply to our compound.

Overall, while specific solubility data for this compound may not be readily available, understanding its structure and functional groups provides a framework to predict its solubility characteristics. Moreover, experimental solubility tests in various solvents would yield valuable insights into its behavior.

Interesting facts

Interesting Facts about Ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate

Ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate is a remarkable compound that falls within the realms of medicinal chemistry and organic synthesis. Below are some intriguing aspects of this compound:

  • Structural Features: This compound possesses a unique thieno[2,3-c]pyridine scaffold, which enhances its potential as a bioactive molecule. The thienopyridine structure is known for its prevalence in various pharmacological activities.
  • Biological Relevance: Compounds featuring the thieno[2,3-c]pyridine core are often investigated for their antimicrobial, anti-inflammatory, and anticancer properties. This makes such derivatives highly relevant in drug discovery.
  • Substituents: The inclusion of an amino group and a benzyl moiety significantly affects the compound's biological activity and solubility. Substituents play a crucial role in modulating the receptor binding and therapeutic effectiveness.
  • Potential Applications: As a synthetic intermediate, this compound can serve as a precursor for developing other bioactive materials, expanding its utility in pharmaceutical research.
  • Research Frontier: Chemists are constantly exploring derivatives of thienopyridines to develop novel compounds with optimized therapeutic profiles. The modifications in its structure could lead to significant advancements in treating various diseases.

As with many complex organic compounds, the interactions of ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate with biological systems are an area of active research. Understanding these interactions through studies in pharmacology and chemical biology can unveil valuable insights into its therapeutic potential.

"The beauty of synthetic chemistry lies in its infinite possibilities for compound design and discovery!"

Synonyms
Tinoridine
24237-54-5
ethyl 2-amino-6-benzyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate
Nonflamin (free base)
Tinoridine [INN]
Tinoridinum
Tinoridino
Y 3642
Tinoridinum [INN-Latin]
Tinoridino [INN-Spanish]
tinoridina
NSC 158555
Y-3642
UNII-C9Z9ICZ7YR
C9Z9ICZ7YR
EINECS 246-102-0
Tinoridine (INN)
ethyl 2-amino-6-benzyl-5,7-dihydro-4H-thieno[2,3-c]pyridine-3-carboxylate
NSC-158555
BRN 1082341
DTXSID9023677
TINORIDINE [MI]
TINORIDINE [WHO-DD]
2-Amino-3-ethoxycarbonyl-6-benzyl-4,5,6,7-tetrahydrothieno(2,3-c)pyridine
Ethyl 2-amino-6-benzyl-4,5,6,7-tetrahydrothieno(2,3-c)pyridine-3-carboxylate
2-Amino-6-benzyl-4,5,6,7-tetrahydrothieno(2,3-c)pyridine-3-carboxylic acid ethyl ester
CHEMBL592943
DTXCID403677
2-Amino-3-aethoxycarbonyl-6-benzyl-4,5,6,7-tetrahydrothieno(2,3-c)pyridin
Ethyl 2-amino-6-benzyl-4,5,6,7-tetrahydrothieno-[2,3-c]pyridine-3-carboxylate
2-Amino-3-aethoxycarbonyl-6-benzyl-4,5,6,7-tetrahydrothieno(2,3-c)pyridin [German]
Thieno(2,3-c)pyridine-3-carboxylic acid, 2-amino-6-benzyl-4,5,6,7-tetrahydro-, ethyl ester
Thieno[2,3-c]pyridine-3-carboxylic acid, 2-amino-4,5,6,7-tetrahydro-6-(phenylmethyl)-, ethyl ester
NCGC00159451-02
Tinoridinum (INN-Latin)
Tinoridino (INN-Spanish)
Ethyl 2-amino-6-benzyl-4,5,6,7-tetrahydrothieno [2,3-c]pyridine-3-carboxylate
Thieno(2,3-c)pyridine-3-carboxylic acid, 4,5,6,7-tetrahydro-2-amino-6-benzyl-, ethyl ester
Thieno(2,3-c)pyridine-3-carboxylic acid, 2-amino-4,5,6,7-tetrahydro-6-(phenylmethyl)-, ethyl ester
tinoridin
Nonflamine
ethyl 2-amino-6-benzyl-4H,5H,6H,7H-thieno[2,3-c]pyridine-3-carboxylate
Ethyl 2-Amino-6-benzyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate (Tinoridine)
CAS-24237-54-5
ethyl 2-amino-6-benzyl-4H,5H,6H,7H-thieno(2,3-c)pyridine-3-carboxylate
2-Amino-3-ethoxycarbonyl-6-benzyl-4,5,6,4-tetrahydrothieno[2,3-c]pyridine; 2-Amino-3-ethoxycarbonyl-6-benzyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine; 2-Amino-3-ethoxycarboxyl-6-benzyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine; NSC 158555; Tinoridine; Y 3642
MFCD00401417
Maybridge2_000001
CBMicro_018439
Oprea1_041651
Oprea1_798781
SCHEMBL24761
MLS004774001
CHEBI:135353
HMS1303A01
ALBB-017033
BCP12825
CCG-6706
Tox21_111678
BBL022232
BDBM50304470
NSC158555
STK036143
AKOS000267028
Tox21_111678_1
DB13001
HY-W032848
2-amino-6-benzyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid ethyl ester
2-amino-6-benzyl-4,5,6,7-tetrahydrothieno(2,3-c)-pyridine-3-carboxylic acid ethyl ester
IDI1_001041
NCGC00159451-03
NCGC00159451-04
NCGC00159451-05
NCGC00159451-06
AC-27457
AS-35595
SMR000103196
BIM-0018431.P001
CS-0076872
NS00027593
EN300-03920
D08602
SBI-0018431.0001
SR-01000644920-1
Q27275368
Z56176137
F1673-2635
Thieno[2, 2-amino-6-benzyl-4,5,6,7-tetrahydro-, ethyl ester
Thieno[2, 2-amino-4,5,6,7-tetrahydro-6-(phenylmethyl)-, ethyl ester
ethyl 2-amino-6-(phenylmethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate
246-102-0
Thieno(2,3-c)pyridine-3-carboxylic acid, 2-amino-4,5,6,7-tetrahydro-6-(phenylmethyl)-, ethyl ester (9CI)
Thieno(2,3-c)pyridine-3-carboxylic acid, 2-amino-6-benzyl-4,5,6,7-tetrahydro-, ethyl ester (8CI)