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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459639생성일: 2026년 10월 24일

Methyl chloroformate → 1-benzyl 4-tert-butyl ((1S)-1-[(5-amino-1-methyl-1H-pyrazol-4-yl)carbamoyl]tetramethylene}biscarbamate

https://huagongshe.com/ko/reaction/459639

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroformateHCID 6586—
반응물TriethylamineHCID 8471—
반응물Z-Ndelta-Boc-L-ornithineHCID 7350734—
반응물1H-Pyrazole, 4,5-diamine-1-methyl-, sulfate (1:1)HCID 21904571—
용매WaterHCID 962—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
생성물1-benzyl 4-tert-butyl ((1S)-1-[(5-amino-1-methyl-1H-pyrazol-4-yl)carbamoyl]tetramethylene}biscarbamateHCID 86597888—

반응 단계

To a solution of (2S)-2-[(benzyloxycarbonyl)amino]-5-[(tert-butoxycarbonyl)amino]pentanoic acid (22.0 g) and triethylamine (6.7 g) in tetrahydrofuran (240 ml) was added methyl chloroformate (6.2 g) followed by stirring under ice-cooling for 30 minutes. To the reaction mixture was added a solution of 1-methyl-1H-pyrazole-4,5-diamine sulfate (12.6 g) and triethylamine (13.4 g) in water (50 ml) at the same temperature. The mixture was stirred at the room temperature for 1 hour. To the reaction mixture was added chloroform (240 ml), and the layers were separated. The organic layer was washed successively with 10% aqueous citric acid solution, brine and saturated aqueous sodium hydrogencarbonate solution. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give a crude product of 1-benzyl 4-tert-butyl {(1S)-1-[(5-amino-1-methyl-1H-pyrazol-4-yl)carbamoyl]tetramethylene}biscarbamate as an oil. The crude product was used directly in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192943B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-9c9e5880ba7c4d1c8e708dfff936c1dc
출처 메모uspto-grants-2007_03