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HRID 56022생성일: 2026년 10월 24일

Methanamine, N-methoxy-, hydrochloride (1:1) → (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate

https://huagongshe.com/ko/reaction/56022

반응식

참여 물질

역할이름HCID투입량
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물Tert-butoxycarbonylalanineHCID 85082—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamateHCID 1180653053.4%

반응 단계

To 20.0 g of N-(tert-butoxycarbonyl)-L-alanine in 352 ml of dichloromethane, 12.4 g of N,O-dimethylhydroxylamine hydrochloride, 15.7 g of 1-hydroxybenzotriazole monohydrate, 24.3 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 42.7 g of triethylamine were added, and the mixture was stirred at room temperature for 1.5 hours. After completion of the reaction, the reaction mixture was washed with 500 ml of saturated aqueous sodium hydrogen carbonate, 500 ml of 1N aqueous hydrochloric acid and 500 ml of water in this order, the resulting organic layer was dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was washed with 200 ml of hexane to obtain 13.1 g of the desired product as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434684B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-7bf2fc40f7d045b3a212eee3617c292a
출처 메모uspto-grants-2016_09