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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1898524생성일: 2026년 10월 25일

Trifluoroacetic acid → HCID 53386254, 화합물

https://huagongshe.com/reaction/1898524

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물PyrrolidineHCID 31268—
반응물BOC-D-alanineHCID 637606—
반응물(2R)-2-{[(tert-butoxy)carbonyl]amino}-3,3-dimethylbutanoic acidHCID 7005057—
반응물Azetidine-3-carbonitrile hydrochlorideHCID 45072465—
반응물2-cyclopropyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acidHCID 57829653—
반응물2-(1-ethyl-1H-pyrazol-4-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[3,2-b]pyrazine-7-carboxylic acidHCID 58438544—
생성물HCID 53386254HCID 53386254—

반응 단계

Prepared according to the procedure outlined in Example 1 substituting 3-cyanoazetidine hydrochloride for pyrrolidine, Boc-D-alanine for Boc-D-tert-leucine, and 2-(1-ethyl-1H-pyrazol-4-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[3,2-b]pyrazine-7-carboxylic acid for 2-cyclopropyl-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid. Trifluoroacetic acid was used in place of hydrochloric acid for all N-Boc deprotection steps. MS: (M+H)+=393.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518945B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-075c867383404a17852c156c6fe363b1
출처 메모uspto-grants-2013_08