반응식
[NH2:1][C:2]1[C:3](=[O:14])[NH:4][C:5](=[S:13])[N:6]([CH2:9][CH:10]([CH3:12])[CH3:11])[C:7]=1[NH2:8].O.[CH:16](O)=[O:17]>>[NH2:8][C:7]1[N:6]([CH2:9][CH:10]([CH3:11])[CH3:12])[C:5](=[S:13])[NH:4][C:3](=[O:14])[C:2]=1[NH:1][CH:16]=[O:17]참가 물질
4
실험 절차
5,6-Diamino-1-isobutyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one (Example 6 (c), 0.25 g, 1.2 mmol) was dissolved in formic acid (1.5 mL) and stirred at ambient temperature for 0.5 h. A pink precipitate started to form after a few minutes. Water was added and the resulting mixture stirred for 10 minutes. The pink solid was collected by filtration, washed with water and dried to yield the title compound (0.25 g, 86%). This material was used without further purification. NMR showed that the product was obtained as a mixture of two tautomers: formamide (major) and imino (minor).
후처리
- customto form after a few minutes
- stirringthe resulting mixture stirred for 10 minutes
- filtrationThe pink solid was collected by filtration
- washwashed with water
- customdried
출처 및 근거
- ORD 기록
- ord-275db70f13ed4edbb5aa05d74088ad08
- 출처 데이터셋
- uspto-grants-2008_09
- 특허 번호
- US07425560B2
연결된 노트
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