Benzyloxyamine hydrochloride → 1-(Benzyloxy)-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)urea
반응식
Cl.[CH2:2]([O:9][NH2:10])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[S:11]1[CH:15]=[CH:14][C:13]2[CH:16]([N:20]=[C:21]=[O:22])[CH2:17][CH2:18][CH2:19][C:12]1=2>>[CH2:2]([O:9][NH:10][C:21]([NH:20][CH:16]1[C:13]2[CH:14]=[CH:15][S:11][C:12]=2[CH2:19][CH2:18][CH2:17]1)=[O:22])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1참가 물질
3
실험 절차
In the manner described in Example 6, O-benzyl hydroxyamine hydrochloride and 4,5,6,7-tetrahydrobenzo[b]thien-4-yl isocyanate are allowed to react to afford 1-(benzyloxy)-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)urea, which is recrystallized from 95% ethyl alcohol-methyl isobutyl ketone. The product melts at 96.5° C. to 99° C.
후처리
- customto react
출처 및 근거
- ORD 기록
- ord-0dcd427e17f2486199d53ee7f6339ced
- 출처 데이터셋
- uspto-grants-1977_07
- 특허 번호
- US04036979
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