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HRID 2272969생성일: 2026년 10월 26일

Triethylamine → 1-tert-butyl-1H-pyrazole-4-carboxylic acid methoxy-methyl-amide

https://huagongshe.com/reaction/2272969

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-tert-Butyl-1H-pyrazole-4-carboxylic acidHCID 24696291—
반응물HCID 178527226HCID 178527226—
용매DichloromethaneHCID 6344—
생성물1-tert-butyl-1H-pyrazole-4-carboxylic acid methoxy-methyl-amideHCID 60491075—

반응 단계

To a suspension of 5.00 g (29.7 mmol) 1-tert-butyl-1H-pyrazole-4-carboxylic acid and 5.80 g (59.5 mmol) N,O-dimethylhydroxylamine hydrochloride in 60 ml dichloromethane are added 12.5 g (65.4 mmol) N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride, 4.42 g (32.7 mmol) 1-hydroxybenzothiazol and 16.5 ml (119 mmol) triethylamine. The reaction mixture is stirred for 18 hours at room temperature. It is quenched with saturated sodium hydrogen carbonate solution and the mixture is partitioned between water and dichloromethane. The organic phase is dried over sodium sulfate and evaporated. The residue is chromatographed on a silica gel column with cyclohexane/ethyl acetate as eluent to afford 1-tert-butyl-1H-pyrazole-4-carboxylic acid methoxy-methyl-amide as colorless crystals; HPLC/MS 1.91 min (B), [M+H] 212.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09120805B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-ea6b68daf65d4710bf6eec751004ee32
출처 메모uspto-grants-2015_09