関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Glucopyranosylamine | HCID 193433 | — |
| 反応物 | o-nitrophenyl N-(2-chloroethyl)N-nitrosocarbamate | HCID 13231923 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosourea | HCID 9972891 | 78.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04156777 |
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| 出典データセット | uspto-grants-1979_05 |
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| ORD ID | ord-f0f3b5deda30497dba7e23e56403c61f |
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| 出典メモ | uspto-grants-1979_05 |
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