1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI)

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1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI) manufacturers

1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI) Basic information
Product Name:1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI)
Synonyms:1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI);1-Methyl-1H-[1,2,4]triazole-3-carboxylicacidmethylester;1-Methyl-1H-[1,2,4]triazole-3-carboxylic acid aMide;1H-1,2,4-Triazole-3-carboxylic acid, 1-methyl-, methyl ester;methyl 1-methyl-1,2,4-triazole-3-carboxylate;Methyl 1-Methyl-1H-1,2,4-triazole-3-carboxylate
CAS:57031-66-0
MF:C5H7N3O2
MW:141.13
EINECS:
Product Categories:CARBOXYLICESTER
Mol File:57031-66-0.mol
1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI) Structure
1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI) Chemical Properties
Boiling point 263℃
density 1.32
Fp 113℃
storage temp. Sealed in dry,Room Temperature
pka0.69±0.10(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C5H7N3O2/c1-8-3-6-4(7-8)5(9)10-2/h3H,1-2H3
InChIKeyNKPPQSVPTZHGMA-UHFFFAOYSA-N
SMILESN1(C)C=NC(C(OC)=O)=N1
Safety Information
MSDS Information
1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI) Usage And Synthesis
Synthesis
Methyl 1,2,4-triazole-3-carboxylate

4928-88-5

Iodomethane

74-88-4

1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI)

57031-66-0

Step A: Preparation of methyl 1-methyl-1H-1,2,4-triazole-3-carboxylate: To a suspension of sodium hydride (60% oil dispersion, 0.346 g, 8.66 mmol) in N,N-dimethylformamide (DMF, 20 mL) under stirring at 0°C under nitrogen protection was slowly added dropwise methyl 1H-1,2,4-triazole-3-carboxylate (1.00 g, a 7.87 mmol) solution in DMF (20 mL). The reaction mixture was continued to be stirred at 0 °C for 1 hour. Subsequently, iodomethane (MeI, 0.982 mL, 15.7 mmol) was added dropwise. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was poured into cold water and extracted with ethyl acetate (EtOAc). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=3:1) to afford the target product methyl 1-methyl-1H-1,2,4-triazole-3-carboxylate (0.380 g, 34% yield) as a white solid. Mass spectrum (APCI) m/z = 142.1 (M + H).

References[1] Chemistry and Biodiversity, 2017, vol. 14, # 12,
[2] Patent: WO2014/78417, 2014, A1. Location in patent: Paragraph 00310
[3] Patent: WO2014/78322, 2014, A1. Location in patent: Paragraph 00430
[4] Patent: WO2014/78325, 2014, A1. Location in patent: Paragraph 00614
[5] Patent: WO2014/78408, 2014, A1. Location in patent: Paragraph 00545
1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI) Preparation Products And Raw materials
Raw materialsMethyl 1,2,4-triazole-3-carboxylate-->1H-1,2,4-Triazole-3-carboxylic acid-->Mineral oil-->Dimethyl sulfate-->Iodomethane-->Sodium hydride-->N,N-Dimethylformamide
Tag:1H-1,2,4-Triazole-3-carboxylicacid,1-methyl-,methylester(9CI)(57031-66-0) Related Product Information
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