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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20156생성일: 2026년 10월 23일

Triethylamine → N-[(2S,6R)-4-(Cyclopropylmethyl)-5-oxo-2-phenyl-1,4-oxazepan-6-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamide

https://huagongshe.com/ko/reaction/20156

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DiisopropylethylamineHCID 81531—
반응물4-Nitrophenyl chloroformateHCID 82129—
반응물1-(piperidin-4-yl)-1H,2H,3H-imidazo[4,5-b]pyridin-2-one dihydrochlorideHCID 22293181—
반응물(2S,6R)-6-amino-4-(cyclopropylmethyl)-2-phenyl-1,4-oxazepan-5-oneHCID 60037869—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N-[(2S,6R)-4-(Cyclopropylmethyl)-5-oxo-2-phenyl-1,4-oxazepan-6-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamideHCID 1128350085.8%

반응 단계

Triethylamine (0.015 mL, 0.109 mmol) was added to a solution of (2S,6R)-6-amino-4-(cyclopropylmethyl)-2-phenyl-1,4-oxazepan-5-one (27 mg, 0.104 mmol) and 4-nitrophenyl chloroformate (22 mg, 0.109 mmol) in tetrahydrofuran (2 mL) at 0° C. After 0.5 h, diisopropylethylamine (0.072 mL, 0.415 mmol), 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine dihydrochloride (36 mg, 0.124 mmol), and dichloromethane (2.5 mL) were added and the mixture warmed to ambient temperature. After 18 h, the mixture was concentrated. Purification by silica gel chromatography (100% dichloromethane→95% dichloromethane/methanol) gave the title compound (45 mg). MS 505.2559 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745427B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7f4610bd0f7043ccb422dfb89a9be381
출처 메모uspto-grants-2010_06