돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423739생성일: 2026년 10월 25일

Water → ({[2-(6-Amino-indol-1-yl)-2-oxo-ethyl]-methyl-carbamoyl}-methyl)-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/423739

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Stannous chloride dihydrateHCID 61436—
반응물DiisopropylethylamineHCID 81531—
반응물Methyl-({methyl-[2-(6-nitro-indol-1-yl)-2-oxo-ethyl]-carbamoyl}-methyl)-carbamic acid tert-butyl esterHCID 66675158—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물({[2-(6-Amino-indol-1-yl)-2-oxo-ethyl]-methyl-carbamoyl}-methyl)-methyl-carbamic acid tert-butyl esterHCID 6667569699.5%

반응 조건

온도70 °C

반응 단계

A mixture of methyl-({methyl-[2-(6-nitro-indol-1-yl)-2-oxo-ethyl]-carbamoyl}-methyl)-carbamic acid tert-butyl ester (12.4 g, 30.6 mmol), SnCl2.2H2O (34.5 g, 153.2 mmol) and DIEA (74.8 mL, 429 mmol) in ethanol (112 mL) was heated to 70° C. for 3 h. Water and EtOAc were added and the mixture was filtered through a short plug of Celite. The organic layer was separated, dried over Na2SO4 and concentrated to yield ({[2-(6-Amino-indol-1-yl)-2-oxo-ethyl]-methyl-carbamoyl}-methyl)-methyl-carbamic acid tert-butyl ester (B-26) (11.4 g, quant.). HPLC ret. time 2.11 min, 10-99% CH3CN, 5 min run; ESI-MS 375.3 m/z (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101767B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8f390b5d6a724bd099ef933ee907f6c7
출처 메모uspto-grants-2012_01