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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1615859생성일: 2026년 10월 26일

Trifluoroacetic acid → (6S)-3-{3-[(8R)-8-(3,5-Difluorophenyl)-6-(2-fluoroethyl)-8-methyl-10-oxo-6,9-diazaspiro[4.5] dec-9-yl]prop-1-yn-1-yl}-5,7-dihydrospiro[cyclopenta[b]pyridine-6,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-one

https://huagongshe.com/reaction/1615859

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물(6S)-3-{3-[(8R)-6-(2-Chloroethyl)-8-(3,5-difluorophenyl)-8-methyl-10-oxo-6,9-diazaspiro[4.5]dec-9-yl]prop-1-yn-1-yl}-5,7-dihydrospiro[cyclopenta[b]pyridine-6,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 66865111—
촉매Caswell No. 736HCID 62656—
용매AcetonitrileHCID 6342—
생성물(6S)-3-{3-[(8R)-8-(3,5-Difluorophenyl)-6-(2-fluoroethyl)-8-methyl-10-oxo-6,9-diazaspiro[4.5] dec-9-yl]prop-1-yn-1-yl}-5,7-dihydrospiro[cyclopenta[b]pyridine-6,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-oneHCID 58118709—

반응 단계

A solution of (6S)-3-{3-[(8R)-6-(2-chloroethyl)-8-(3,5-difluorophenyl)-8-methyl-10-oxo-6,9-diazaspiro[4.5] dec-9-yl]prop-1-yn-1-yl}-5,7-dihydrospiro[cyclopenta[b]pyridine-6,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one from Step A (67 mg, 0.11 mmol) and silver(I)fluoride (140 mg, 1.1 mmol) in acetonitrile (3 ml) was heated at 100° C. for 90 min The mixture was diluted with TFA (0.5 mL), filtered, and purified directly by HPLC using a reversed phase C18 column and eluting with a gradient of H2O:CH3CN:CF3CO2H—90:10:0.1 to 5:95:0.1. The desired fractions were poured onto saturated NaHCO3 (10 mL) and extracted with CH2Cl2 (3×10 ml). The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo to yield the title compound. MS: m/z=600 (M+1). HRMS: m/z=600.2604 (M+1); calculated m/z=600.2581 (M+1) for C34H34F3N5O2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765759B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-abecab5383284c299f73ec99b40c847b
출처 메모uspto-grants-2014_07