돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2237406생성일: 2026년 10월 26일

Sodium hydride → 2-chloro-N-(5-chloro-1,3-benzodioxol-4-yl)pyrimidin-4-amine

https://huagongshe.com/reaction/2237406

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2,4-DichloropyrimidineHCID 77531—
반응물5-Chloro-1,3-benzodioxol-4-amineHCID 11367253—
용매DimethylacetamideHCID 31374—
생성물2-chloro-N-(5-chloro-1,3-benzodioxol-4-yl)pyrimidin-4-amineHCID 42631684—

반응 단계

Sodium hydride (13.4 g, 60% dispersion in mineral oil) was added portionwise to (5-chloro-1,3-benzodioxol-4-yl)amine (11.5 g, prepared as described in WO2001094341) in DMA (100 ml) at 0° C. 2,4-Dichloropyrimidine (10 g) was added and the reaction warmed to room temperature and stirred overnight. The reaction was quenched cautiously with water, the solution filtered and concentrated and the residue dissolved in DCM, washed with water and brine, dried and concentrated to give 2-chloro-N-(5-chlorobenzo[d][1,3]dioxol-4-yl)pyrimidin-4-amine as a dark brown oil that was used without further purification (16 g, 85%); NMR Spectrum (300 MHz, DMSO) 6.10 (s, 2H), 6.58 (d, 1H), 6.94 (d, 1H), 7.05 (d, 1H), 8.15 (d, 1H), 9.76 (s, 1H); Mass Spectrum M+ 284.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07718653B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-f82a01ee902b4b9bab48dbf01b09e4c3
출처 메모uspto-grants-2010_05