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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 405980생성일: 2026년 10월 25일

Ammonia → 4-Amino-6-chloropyrimidine-5-carbonitrile

https://huagongshe.com/reaction/405980

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물4,6-Dichloropyrimidine-5-carbonitrileHCID 599371—
용매TetrahydrofuranHCID 8028—
생성물4-Amino-6-chloropyrimidine-5-carbonitrileHCID 12278262—

반응 단계

The white solid, 4,6-dichloropyrimidine-5-carbonitrile (5.82 g, 33.5 mmol) was dissolved in THF (66.9 mL) in a 500 mL round-bottom flask and to the mixture was bubbled through ammonia gas (0.570 g, 33.5 mmol) for 3 min in 10 min intervals with stirring. After 50 min, a white precipitate (ammmonium chloride) was filtered and the solid was washed with THF (100 mL). To the filtrate was added silica gel and concd under reduced pressure. The mixture was purified by silica gel column chromatography on a 120 g of Redi-Sep™ column using 0 to 100% gradient of EtOAc in hexane over 27 min and then 100% isocratic of EtOAc in hexane for 20 min as eluent to give 4-amino-6-chloropyrimidine-5-carbonitrile as an off-white solid. The off-white solid was suspended in EtOAc-hexane (1:1, 20 mL), filtered, washed with EtOAc-hexane (1:1, 30 mL), and dried to give 4-amino-6-chloropyrimidine-5-carbonitrile as a white solid: 1H NMR (500 MHz, DMSO-d6) δ ppm 7.91-8.77 (3 H, m); Mass Spectrum (ESI) m/e=154.9 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754089B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-2aad595623ec460cb17a9e534649b2f1
출처 메모uspto-grants-2014_06