돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 524323생성일: 2026년 10월 25일

2-Naphthoic acid → N-(2-(methoxy(methyl)amino)-2-oxoethyl)-2-naphthamide

https://huagongshe.com/reaction/524323

반응식

참여 물질

역할이름HCID투입량
반응물2-Naphthoic acidHCID 7123—
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물Sodium BicarbonateHCID 516892—
반응물2-amino-N-methoxy-N-methylacetamideHCID 10329278—
용매DichloromethaneHCID 6344—
생성물N-(2-(methoxy(methyl)amino)-2-oxoethyl)-2-naphthamideHCID 45866900—

반응 단계

To a mixture of 2-naphthoic acid (5.8 g, 33.7 mmol), 2-amino-N-methoxy-N-methylacetamide (Gly Weinreb amide; prepared from Boc-Gly Weinreb amide 15 as in Example 43) (3.8 g, 32.1 mmol) and DIPEA (12.0 mL, 68.9 mmol) in DCM (70 mL) was added BOP (14.9 g, 33.7 mmol) in one portion at room temperature. The resulting mixture was stirred for 1 hr then saturated NaHCO3 aqueous solution was added. The organic layer was washed with brine (5×60 mL) and 1 N HCl (2×30 mL), dried over MgSO4, filtered and concentrated under reduced pressure to give the crude product, which was used in the next reaction without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340517B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-2fae8f2338064ab1a1a6fe55ea671e8c
출처 메모uspto-grants-2016_05