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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 573064생성일: 2026년 10월 26일

Triethylamine → (Z)-tert-butyl 5-(benzyloxy)-3-(3-morpholino-3-oxoprop-1-enyl)-1H-indole-1-carboxylate

https://huagongshe.com/reaction/573064

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Tri-o-tolylphosphineHCID 80271—
반응물AcryloylmorpholineHCID 98723—
반응물5-(Benzyloxy)-3-bromo-1H-indole, N-BOC protectedHCID 40428554—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
용매Ammonium ChlorideHCID 25517—
생성물(Z)-tert-butyl 5-(benzyloxy)-3-(3-morpholino-3-oxoprop-1-enyl)-1H-indole-1-carboxylateHCID 67227351—

반응 조건

온도100 °C

반응 단계

A mixture of tert-butyl 5-(benzyloxy)-3-bromo-1H-indole-1-carboxylate (2.011 g), 1-morpholinoprop-2-en-1-one (0.776 g), palladium acetate (31 mg), tri-o-tolylphosphine (187 mg) and triethylamine (1.14 mL) in N,N-dimethylformamide (14 mL) under nitrogen atmosphere was stirred at 100° C. overnight. The mixture was diluted with ethyl acetate and saturated ammonium chloride. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography (80% ethyl acetate-hexane) to give the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029404B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-73b57b0cfd00485b8716c6d5aa974531
출처 메모uspto-grants-2015_05