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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 515953생성일: 2026년 10월 25일

Triethylamine → Methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/515953

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(1S,2R)-Cyclohexane-1,2-diamine, N1-BOC protectedHCID 1514389—
반응물Methyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 58317549—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물Methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylateHCID 6723801562.2%

반응 단계

A solution of methyl 2-chloro-4-methyl-6-(m-tolylamino)pyrimidine-5-carboxylate (1.2 g, 4.11 mmol), tert-butyl (1S,2R)-2-aminocyclohexylcarbamate (0.882 g, 4.11 mmol) and triethylamine (1.720 mL, 12.34 mmol) in DMA (10 mL) was heated at 90° C. for 4 h. The solution was then diluted with EtOAc, washed with brine and water. The organic extract was dried and concentrated under reduced pressure to give a light yellow residue; white crystals were formed upon triturating with ACN (5 mL). The resultant solid was filtered, washed with ACN, and dried to give the title compound as white solid (1.2 g, 62%). [M+H] calc'd for C25H35N5O4, 470; found, 470.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108970B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-805520152a0b406485e703eae335253d
출처 메모uspto-grants-2015_08