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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 711495생성일: 2026년 10월 26일

Triethylamine → Methyl 2-(3-(tert-butoxycarbonylamino)prop-1-ynyl)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/711495

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
반응물Methyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 58317549—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매DimethylacetamideHCID 31374—
생성물Methyl 2-(3-(tert-butoxycarbonylamino)prop-1-ynyl)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 5831751334%

반응 조건

온도90 °C

반응 단계

Methyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate (0.4 g, 1.371 mmol), tert-butyl prop-2-ynylcarbamate (0.426 g, 2.74 mmol), tetrakis(triphenylphosphine)palladium (0.032 g, 0.027 mmol), and copper (I) iodide (0.026 g, 0.137 mmol) was dispersed in DMA (5 mL). Triethylamine (0.382 mL, 2.74 mmol) was added and the mixture was degassed with nitrogen for 5 min. The reaction mixture was placed in a sealed tube and heated at 90° C. for 4 h, after which it was filtered through a pad of Celite, which was rinsed with MeOH. The filtrate was purified via reverse phase preparative HPLC and the fractions were concentrated in vacuo to give the title compound as a brown oil (0.190 g, 34%). [M+H] calc'd for C22H26N4O4, 411. found, 411.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181255B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-af85f13051654d38bb8802ef8d546630
출처 메모uspto-grants-2015_11