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HRID 263357作成日:2026年10月27日

Glucopyranosylamine → N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosourea

https://huagongshe.com/reaction/263357

反応式

関与物質

役割名称HCID仕込み量
反応物GlucopyranosylamineHCID 193433—
反応物o-nitrophenyl N-(2-chloroethyl)N-nitrosocarbamateHCID 13231923—
溶媒EthanolHCID 702—
溶媒DimethylformamideHCID 6228—
生成物N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosoureaHCID 997289178.7%

反応手順

3.28 g (12 mmol) of o-nitrophenyl N-(2-chloroethyl)-N-nitrosocarbamate is dissolved in a mixture of 10 ml anhydrous dimethylformamide and 10 ml anhydrous ethanol, and to this solution is added little by little 1.79 g (10 mmol) of 1-amino-1-deoxy-β-D-glucopyranose powder, while stirring, at 5°-10° C. over 10 minutes. The resultant mixture is, after adding 5 ml of anhydrous dimethylformamide thereto, stirred further at 10° C. for 5 hours, and the thus reacted solution is concentrated at 40° C. and below, under reduced pressure. The crystalline residue obtained is washed with anhydrous ethyl ether and then with acetone, dried under reduced pressure, and recrystallized from anhydrous ethanol-ethyl ether (1:5) to give 2.47 g of 3-(β-D-glucopyranosyl)-1-(2-chloroethyl)-1-nitrosourea. Yield 78.7%. mp 77°-78° C. (decomp.). [α]D25 -10.3° (C 1.0, water). Analysis for C9H16N3O7Cl (MW 313.69):

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04156777
出典データセットuspto-grants-1979_05
ORD IDord-f0f3b5deda30497dba7e23e56403c61f
出典メモuspto-grants-1979_05