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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241674생성일: 2026년 10월 26일

Chlorotrimethylsilane → (R)-N,N-dimethyl-2-(2-neopentyl-5-(pyrrolidin-3-ylsulfonyl)-1H-benzo[d]imidazol-1-yl)ethanamine

https://huagongshe.com/reaction/241674

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참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물(R)-tert-butyl 3-(1-(2-(dimethylamino)ethyl)-2-neopentyl-1H-benzo[d]imidazol-5-ylsulfonyl)pyrrolidine-1-carboxylateHCID 58513604—
용매MethanolHCID 887—
생성물(R)-N,N-dimethyl-2-(2-neopentyl-5-(pyrrolidin-3-ylsulfonyl)-1H-benzo[d]imidazol-1-yl)ethanamineHCID 5851358593.1%

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온도50 °C

반응 단계

To a solution of (R)-tert-butyl 3-(1-(2-(dimethylamino)ethyl)-2-neopentyl-1H-benzo[d]imidazol-5-ylsulfonyl)pyrrolidine-1-carboxylate (STEP B, 612 mg, 1.24 mmol) in methanol (5 mL) was added chlorotrimethylsilane (749 microL, 6.21 mmol). The mixture was stirred at 50° C. for 3 h. The mixture was concentrated in vacuo. To the residue was added 2 mol/L sodium hydroxide aqueous solution to pH>7 and the mixture was extracted with ethyl acetate (150 mL). The organic layer was washed with brine and dried over sodium sulfate. The resulting solution was concentrated to give the title compound (453 mg, 93%) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653063B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-d519c11abe5146429d739ddd8bed1bf6
출처 메모uspto-grants-2014_02