Dichloromethane → 9-(Cyclohexylmethyl)-2-(3-hydroxyphenyl)-8-oxo-8,9-dihydro-7H-purine-6-carboxamide
반응식
[NH2:1]/[C:2](/[C:17]#[N:18])=[C:3](\[NH:6][C:7]([NH:9][CH2:10][CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1)=[O:8])/[C:4]#[N:5].N/[C:20](=[C:23](\N)/C#N)/[C:21]#N.N(CC1CCCCC1)=C=[O:29].ClCCl.[O:40]1[CH2:44][CH2:43][CH2:42][CH2:41]1>>[CH:11]1([CH2:10][N:9]2[C:7](=[O:8])[NH:6][C:3]3[C:4]2=[N:5][C:41]([C:42]2[CH:23]=[CH:20][CH:21]=[C:44]([OH:40])[CH:43]=2)=[N:1][C:2]=3[C:17]([NH2:18])=[O:29])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1참가 물질
6
반응물 5
생성물 1
실험 절차
(Z)-1-(2-Amino-1,2-dicyanovinyl)-3-(cyclohexylmethyl)urea. 2,3-Diaminomaleonitrile (0.119 g, 1.10 mmol) and (isocyanatomethyl)cyclohexane (0.140 g, 1.00 mmol) in tetrahydrofuran (2 mL) were reacted according to General Procedure A. Dichloromethane and hexanes were added to the solution and the resultant precipitate was filtered and dried to afford the title compound (0.200 g, 47%). MS (ESI) m/z 248.2 [M+1]+.
후처리
- filtrationthe resultant precipitate was filtered
- customdried
출처 및 근거
- ORD 기록
- ord-762ae629ad1342e6b1665755ac5b6dba
- 출처 데이터셋
- uspto-grants-2013_02
- 특허 번호
- US08383634B2
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