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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38230생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/38230

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물1-[(4-methoxyphenyl)methyl]-1H-pyrazole-4-carboxylic acidHCID 43565362—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-methoxy-1-(4-methoxybenzyl)-N-methyl-1H-pyrazole-4-carboxamideHCID 8664232898.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524718B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1a49b91c957744b1b47ec64285602453
출처 메모uspto-grants-2013_09