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HRID 38230作成日:2026年10月26日

Triethylamine → N-methoxy-1-(4-methoxybenzyl)-N-methyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/38230

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物1-[(4-methoxyphenyl)methyl]-1H-pyrazole-4-carboxylic acidHCID 43565362—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-methoxy-1-(4-methoxybenzyl)-N-methyl-1H-pyrazole-4-carboxamideHCID 8664232898.3%

反応手順

According to Scheme 3 Step 1: A solution of 1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylic acid (34.4 mmol, 8.00 g), oxalyl chloride (68.9 mmol, 5.92 mL) and a drop of DMF in DCM (80 mL) was stirred for 1 hour at room temperature. After evaporation, the crude product was dissolved in DCM (30 mL) and was added at 0° C. to a solution of N,O-dimethylhydroxylamine hydrochloride (103 mmol, 6.31 g) in DCM (100 mL) followed by Et3N (138 mmol, 19.2 mL). The reaction mixture was stirred for 1 hour at room temperature. The reaction was quenched with a saturated solution of Na2CO3 (300 mL) and the aqueous phase was extracted with DCM. The organic phase was dried over MgSO4, was filtered and was concentrated to yield N-methoxy-1-(4-methoxybenzyl)-N-methyl-1H-pyrazole-4-carboxamide (33.8 mmol, 9.30 g, 98%) as a beige solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524718B2
出典データセットuspto-grants-2013_09
ORD IDord-1a49b91c957744b1b47ec64285602453
出典メモuspto-grants-2013_09