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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2093119생성일: 2026년 10월 26일

Triethylamine → tert-butyl 2-({2-[(tert-butoxycarbonyl)amino]phenyl} carbamoyl)-1,4,6,7-tetrahydro-5H-pyrrolo[3,2-c]pyridine-5-carboxylate

https://huagongshe.com/reaction/2093119

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-(tert-Butoxycarbonyl)-1,2-phenylenediamineHCID 676311—
반응물5-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acidHCID 66523307—
용매DimethylformamideHCID 6228—
생성물tert-butyl 2-({2-[(tert-butoxycarbonyl)amino]phenyl} carbamoyl)-1,4,6,7-tetrahydro-5H-pyrrolo[3,2-c]pyridine-5-carboxylateHCID 66864448—

반응 단계

To a solution of compound 5-(tert-butoxycarbonyl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid (1.0 eq) in DMF was added triethyl amine (2.2 eq), Bis (2-oxo-3-oxazolidinyl) phosphonic chloride (BOP, 1.2 eq.) and stirred for 1 hr. Monoboc phenylene diamine was added and reaction was stirred for 24 hrs. Reaction mixture was then quenched with water and extracted with ethyl acetate, dried over sodium sulphate and concentrated to dryness. Crude mass was then purified by silica gel column chromatography to afford tert-butyl 2-({2-[(tert-butoxycarbonyl)amino]phenyl}carbamoyl)-1,4,6,7-tetrahydro-5H-pyrrolo[3,2-c]pyridine-5-carboxylate, which was then reacted with hydrochloric acid saturated diethyl ether to get N-(2-aminophenyl)-4,5,6,7-tetrahydro-1H-pyrrolo[3,2]pyridine-2-carboxamide

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08440830B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-21c41703363e443fb79a2154fcdd4574
출처 메모uspto-grants-2013_05