돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450390생성일: 2026년 10월 26일

Diisopropylethylamine → 2-Chloro-N-(5-methyl-1H-pyrazol-3-yl)-5-nitro-N-(tetrahydro-2H-pyran-4-yl)pyrimidine-4,6-diamine

https://huagongshe.com/reaction/450390

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
반응물2,4,6-Trichloro-5-nitropyrimidineHCID 4297843—
반응물2H-pyran-4-amineHCID 17791271—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-Chloro-N-(5-methyl-1H-pyrazol-3-yl)-5-nitro-N-(tetrahydro-2H-pyran-4-yl)pyrimidine-4,6-diamineHCID 86649284—

반응 단계

To a solution of 2,4,6-trichloro-5-nitro pyrimidine (Intermediate 37, 1 g, 4.4 mmol) in EtOH at −50° C. were added 5-methyl-1H-pyrazol-3-amine (255 mg) and DIPEA (1.6 ml) drop-wise. The resulting mixture was stirred at this temperature for 5 minutes whereupon 4-amino pyran (300 mg) was added. The resulting mixture was allowed to warm to ambient temperature for 4 hours. The mixture was diluted with H2O and EtOAc and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, saturated NaHCO3 (aq) solution, dried and evaporation of the volatiles under reduced pressure gave a colored residue. Purification by Gilson (MeCN/H2O, 5%→95%, 15 minutes) gave the title compound (120 mg). LCMS: 354 [M+1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486966B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-0cac8eba3950473ca5dbaaedd86949aa
출처 메모uspto-grants-2013_07