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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535404생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → tert-butyl-N-methyl-N-[1-[[5-(oxane-4-carbonylamino)-6-(2-phenylethynyl)-pyridin-2-yl]amino]-1-oxopropan-2-yl]carbamate

https://huagongshe.com/reaction/535404

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물DiisopropylethylamineHCID 81531—
반응물2-(((Tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 4436857—
반응물N-[6-amino-2-(2-phenylethynyl)pyridin-3-yl]oxane-4-carboxamideHCID 86694381—
용매DichloromethaneHCID 6344—
생성물tert-butyl-N-methyl-N-[1-[[5-(oxane-4-carbonylamino)-6-(2-phenylethynyl)-pyridin-2-yl]amino]-1-oxopropan-2-yl]carbamateHCID 86694390—

반응 단계

A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (34 mg, 0.17 mmol) and N,N′-dicyclohexylcarbodiimide (17 mg, 0.08 mmol) in DCM (1 ml) is stirred at RT for 20 minutes. This mixture is added to N-[6-amino-2-(2-phenylethynyl)pyridin-3-yl]oxane-4-carboxamide D5b (28 mg, 0.09 mmol) and DIPEA (17 μl; 0.10 mmol) in DCM (1 ml). After stirring for 6 days at 40° C. the reaction mixture is diluted with DCM and extracted with water. The combined organic layers are dried over MgSO4 to and concentrated in vacuo. The crude product (70 mg) is used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859541B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-24f9cf2dbfd94776823c52c10e06e1b4
출처 메모uspto-grants-2014_10