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HRID 263363作成日:2026年10月26日

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

https://huagongshe.com/reaction/263363

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物Citric AcidHCID 311—
反応物GlucopyranosylamineHCID 193433—
反応物o-nitrophenyl N-(2-chloroethyl)N-nitrosocarbamateHCID 13231923—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
溶媒1,4-DioxaneHCID 31275—
生成物N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosoureaHCID 997289181.6%

反応手順

1.79 g (10 mmol) of 1-amino-1-deoxy-β-D-glucopyranose is dissolved in a mixture of 20 ml methanol and 10 ml dioxane, and to this solution is added a mixture of formic acid and citric acid dropwise, with stirring, to adjust the PH of the solution to 9.1. The resulting solution is then added dropwise to a solution prepared by dissolving 3.28 g (12 mmol) of o-nitrophenyl N-(2-chloroethyl)-N-nitrosocarbamate in a mixture of 10 ml tetrahydrofuran and 15 ml dioxane, while stirring, at 5°-10° C. over 30 minutes. The resultant mixture is stirred at the same temperature for a further 4 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 (4:1) to give 2.56 g of 3-(β-D-glucopyranosyl)-1-(2-chloroethyl)-1-nitrosourea. Yield 81.5%. 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-9135feff2ddc457486749a511c3e74ee
出典メモuspto-grants-1979_05