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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720113생성일: 2026년 10월 23일

Triethylamine → 2-Ethylsulfanyl-n-(6-oxo-2-phenyl-5,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)-nicotinamide

https://huagongshe.com/ko/reaction/720113

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-(Ethylthio)nicotinic acidHCID 591734—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물8-Amino-2-phenyl-1,5-dihydro-[1,2]diazepino[4,5,6-cd]indol-6-oneHCID 135774079—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-Ethylsulfanyl-n-(6-oxo-2-phenyl-5,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)-nicotinamideHCID 13543410017%

반응 단계

Preparation of example 66 from the title compound of Example 7 (hydrochloride) (30 mg, 0.096 mmol), 2-ethylsulfanyl-nicotinic acid (22 mg, 0.12 mmol), triethylamine (0.020 mL, 0.14 mmol), and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (46 mg, 0.12 mmol) in CH2Cl2 (0.4 mL) and N,N-dimethylformamide (0.4 mL) was carried out analogously to Example 11. Silica gel chromatography (pre-rinsed silica with 3% triethylamine in ethyl acetate, eluted with 3% triethylamine in 19:6:1 ethyl acetate:hexane:methanol), also in an analogous manner, afforded the title compound (7 mg, 0.016 mmol) as a yellow powder in 17% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07132533B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-5c4182fe88244e49b09d1e575f231fec
출처 메모uspto-grants-2006_11