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HRID 2272969作成日:2026年10月26日

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

https://huagongshe.com/reaction/2272969

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-tert-Butyl-1H-pyrazole-4-carboxylic acidHCID 24696291—
反応物HCID 178527226HCID 178527226—
溶媒DichloromethaneHCID 6344—
生成物1-tert-butyl-1H-pyrazole-4-carboxylic acid methoxy-methyl-amideHCID 60491075—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09120805B2
出典データセットuspto-grants-2015_09
ORD IDord-ea6b68daf65d4710bf6eec751004ee32
出典メモuspto-grants-2015_09