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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1417971생성일: 2026년 10월 26일

Sodium hydride → 5-benzyloxy-4-methyl-9-(2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl)-9H-pyrido[3,4-b]indole-3-carboxylic acid-(1-methylethyl)-ester

https://huagongshe.com/reaction/1417971

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물N-methyl-N-phenethyl-2-bromoacetamideHCID 10753531—
반응물5-benzyloxy-4-methyl-9H-pyrido[3,4-b]indole-3-carboxylic acid-(1-methylethyl)-esterHCID 54187064—
용매TetrahydrofuranHCID 8028—
생성물5-benzyloxy-4-methyl-9-(2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl)-9H-pyrido[3,4-b]indole-3-carboxylic acid-(1-methylethyl)-esterHCID 8675386377%

반응 조건

온도0 °C

반응 단계

A solution of 1.096 g of 5-benzyloxy-4-methyl-9H-pyrido[3,4-b]indole-3-carboxylic acid-(1-methylethyl)-ester (2.93 mmol) in 2.9 ml of tetrahydrofuran is added to a suspension of 92.2 mg of sodium hydride (3.03 mmol; 80% in mineral oil) at 0° C. under nitrogen, and it is stirred for 10 minutes at 0° C. Then, 750 mg (2.93 mmol) of N-methyl-N-phenylethyl-2-bromoacetamide is added, and it is then stirred for 18 hours at 24° C. It is filtered off on Celite, the filtrate is concentrated by evaporation in a vacuum, and the crude product that is thus obtained is purified on a silica gel column with hexane/0-100% ethyl acetate. In this way, 1.24 g of 5-benzyloxy-4-methyl-9-(2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl)-9H-pyrido[3,4-b]indole-3-carboxylic acid-(1-methylethyl)-ester is obtained as an amorphous, yellowish-colored solid with a melting point of 69°-74° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05880126
출처 데이터셋uspto-grants-1999_03
ORD IDord-1bc8f937dc24454dbc755016e4c1448a
출처 메모uspto-grants-1999_03