Methyl 5-aminopyridine-3-carboxylate
Methyl 5-aminopyridine-3-carboxylate Basic information
- Product Name:
- Methyl 5-aminopyridine-3-carboxylate
- Synonyms:
-
- METHYL 5-AMINONICOTINATE
- 5-AMINO-NICOTINIC ACID METHYL ESTER
- Methyl 5-aminopyridine-3-carboxylate ,98%
- 5-Aminopyridine-3-carboxylic acid methyl ester
- methyl 5-aminopyridine-3-carboxylate
- Methyl 5-amino-3-pyridinecarboxylate
- 5-Aminopyridine-3-carboxylic acid methyl ester ,98%
- 3-Pyridinecarboxylicacid,5-amino-,methylester
- CAS:
- 36052-25-2
- MF:
- C7H8N2O2
- MW:
- 152.15
- Product Categories:
-
- pharmacetical
- Mol File:
- 36052-25-2.mol
Methyl 5-aminopyridine-3-carboxylate Chemical Properties
- Melting point:
- 135-137℃
- Boiling point:
- 319.4±22.0 °C(Predicted)
- Density
- 1.238
- storage temp.
- 2-8°C
- pka
- 4.13±0.20(Predicted)
- form
- solid
- Appearance
- Light brown to yellow Solid
- BRN
- 128569
- InChI
- InChI=1S/C7H8N2O2/c1-11-7(10)5-2-6(8)4-9-3-5/h2-4H,8H2,1H3
- InChIKey
- MBGSRKHDEJNWED-UHFFFAOYSA-N
- SMILES
- C1=NC=C(N)C=C1C(OC)=O
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-26
- Safety Statements
- 26-36/37/38
- WGK Germany
- 3
- HS Code
- 29339900
Methyl 5-aminopyridine-3-carboxylate Usage And Synthesis
Uses
It is used in organic synthesis and can be used as a starting material for the synthesis of 5-(hydroxymethyl)pyridine-3-ol.
Chemical Properties
Off-white solid
Synthesis
67-56-1
24242-19-1
36052-25-2
SOCl2 (10.4 g, 86.9 mmol) was slowly added dropwise to a stirred methanolic solution (100 mL) of 5-aminonicotinic acid (10.0 g, 72.5 mmol) at 0 °C. After gradually warming the reaction mixture to room temperature, the reaction was continued at reflux for 16 hours. After completion of the reaction, the mixture was cooled and concentrated under vacuum. The residue was diluted with deionized water (200 mL) and subsequently neutralized with aqueous NaHCO3 to pH=7. The aqueous phase mixture was extracted with dichloromethane (DCM, 100 mL x 2). The organic layers were combined, washed with saturated saline (100 mL × 2), dried over anhydrous Na2SO4, filtered, and the filtrate was concentrated to dryness under vacuum to give 9.5 g of methyl 5-aminopyridine-3-carboxylate as a white solid in 86% yield. The product was characterized by 1H NMR (DMSO-d6, 400 MHz): δ=8.24 (1H, d), 8.12 (1H, d), 7.42 (1H, dd), 5.65 (2H, brs), 3.84 (3H, s).
References
[1] Patent: WO2013/126608, 2013, A1. Location in patent: Paragraph 00492-00493
[2] Patent: WO2006/117549, 2006, A1. Location in patent: Page/Page column 97
[3] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 22, p. 6305 - 6310
[4] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 17, p. 6340 - 6350
[5] Chemistry - A European Journal, 2002, vol. 8, # 5, p. 1218 - 1226
Methyl 5-aminopyridine-3-carboxylate Preparation Products And Raw materials
Raw materials
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Methyl 5-aminopyridine-3-carboxylate(36052-25-2)Related Product Information
- 3-METHOXYCARBONYL-5-NITRO-2(1H)-PYRIDINONE
- ETHYL 2-METHYL-5-NITRONICOTINATE
- Methyl-6-chloro-5-nitronicotinate
- 2-CHLORO-5-NITRONICOTINIC ACID METHYL ESTER
- 2-CHLORO-5-NITRONICOTINIC ACID ETHYL ESTER
- 5-AMINO-NICOTINIC ACID METHYL ESTER
- 4-Amino-nicotinic acid methyl ester ,97%
- 2-AMINO-NICOTINIC ACID METHYL ESTER
- 3-AMINO-ISONICOTINIC ACID METHYL ESTER
- Methyl 2-aminopyridine-4-carboxylate
- 3-Aminopyridine-2-carboxylic acid methyl ester
- 5-Aminonicotinic acid
- 4,6-Dihydroxy-5-nitropyridine-3-carboxylic acid ethyl ester
- 5-Amino-6-chloro-3-pyridinecarboxylic acid methyl ester
- methyl 6-amino-5-nitropyridine-3-carboxylate
- 5-AMINO-2-CHLORO-NICOTINIC ACID ETHYL ESTER
- 4,6-Dichloro-5-nitronicotinic acid ethyl ester
- TERT-BUTYL 5-AMINOPYRIDINE-3-CARBOXYLATE