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HRID 1051807作成日:2026年10月25日

4-Methylmorpholine → HCID 89827923、化合物

https://huagongshe.com/reaction/1051807

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
反応物N-alpha-Benzyloxycarbonyl-D-valineHCID 712434—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 89827923HCID 8982792399.5%

反応条件

温度-15 °C

反応手順

A solution of Cbz-D-Valine (500 g, 1.99 mol) and N-methylmorpholine (201.8 g, 1.99 mol) in anhydrous THF (8 L) was cooled to −15° C. and i-butyl chlorofomate (299 g, 2.19 mol) was added dropwise under stirring. After 30 min, a solution of 1-amino-2,2-dimethyoxyethane (209.5 g, 1.99 mol) in THF (1 L) was added slowly and the temperature was maintained at −15° C. for 2 h. The reaction mixture was washed with brine (2 L) and the organic phase was concentrated to remove the THF. The residue was diluted with EtOAc (4 L), washed with 1N aq HCl (2×2 L), sat. aq. NaHCO3 (2 L) and sat. aq. Na2CO3 (2 L) and brine (1.5 L). After drying over Na2SO4, the organic solvent was removed under reduce pressure to afford (R)-benzyl (1-((2,2-dimethoxyethyl)amino)-3-methyl-1-oxobutan-2-yl)carbamate as a white solid (670 g, yield 99.5%), which was used for next step without further purification. LC-MS m/z 360.9 [M+Na]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09388190B2
出典データセットuspto-grants-2016_07
ORD IDord-bfee45d059e94e5285f666db0896a4f1
出典メモuspto-grants-2016_07