참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Glucopyranosylamine | HCID 193433 | — |
| 반응물 | o-nitrophenyl N-(2-chloroethyl)N-nitrosocarbamate | HCID 13231923 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosourea | HCID 9972891 | 78.7% |
반응 단계
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):
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04156777 |
|---|
| 출처 데이터셋 | uspto-grants-1979_05 |
|---|
| ORD ID | ord-f0f3b5deda30497dba7e23e56403c61f |
|---|
| 출처 메모 | uspto-grants-1979_05 |
|---|