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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6529생성일: 2026년 10월 23일

Tri-o-tolylphosphine → HCID 178418607, 화합물

https://huagongshe.com/ko/reaction/6529

반응식

참여 물질

역할이름HCID투입량
반응물Tri-o-tolylphosphineHCID 80271—
반응물diethyl (2S)-2-[(4-iodobenzoyl)amino]pentanedioateHCID 1885228—
반응물ethyl N-(4-iodobenzoyl)glutamateHCID 86747251—
반응물HCID 178418674HCID 178418674—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
용매TriethylamineHCID 8471—
생성물HCID 178418607HCID 178418607—

반응 단계

A mixture containing 3.48 g of 3-(3-tetrahydropyr-2-yloxyprop-1-en-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 3.12g (1.2 equiv.) of diethyl N-(4-iodobenzoyl)glutamate, 546 mg (20%) of tris-(2-methylphenyl)phosphine, 201 mg (10%) of palladium acetate and 85.5 mg (5%) of cuprous iodide in 15 ml of triethylamine and 240 ml of acetonitrile is heated at reflux under nitrogen. After 12 hours., 1.17 g of ethyl N-(4-iodobenzoyl)glutamate are added and the reaction mixture is heated at reflux under nitrogen for an additional 12 hours. The reaction mixture then is concentrated under reduced pressure and the residue chromatographed on silica gel, eluting with 20:1 ethyl acetate:hexane. (Any recovered starting material can be recycled through the foregoing procedure.) The concentrated material is dissolved in 1:5 ethyl acetate:ether and this solution is refrigerated for 15 hours. The solid which forms is collected by filtration, washed with cold ethyl acetate and dried to yield diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248775
출처 데이터셋uspto-grants-1993_09
ORD IDord-f4b94ff8ba9e4c06ac8d51b313e46253
출처 메모uspto-grants-1993_09