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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19845생성일: 2026년 10월 24일

Methyl chloroformate → 2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indole-1-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/19845

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroformateHCID 6586—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indole-1-carboxylic acid methyl esterHCID 1673941115.7%

반응 단계

A solution of (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1, 100 mg, 1.0 eq.), lithium bis-(trimethylsilyl)amide (1M solution in tetrahydrofuran, 271 ul, 1.1 eq.) and methylchloroformate (26 mg, 1.1 eq.) in tetrahydrofuran (2 mL) was stirred at room temperature for 48 h, then poured into brine, extracted with dichloromethane, dried over sodium sulfate, filtered, evaporated to dryness and purified on silica gel, eluting with a 98:2 to 97:3 gradient of dichloromethane/methanol, to yield 18 mg (15%) of the desired product as yellow oil. MS (m/e): 464.2 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0b28f7277bb243879e98cc1ec3c71219
출처 메모uspto-grants-2010_06