1-(1,3-Benzodioxol-5-yl)-1-isopropylurea → 1-Isopropyl-6,7-methylenedioxy-4-(2-chloro-4,5-methylenedioxyphenyl)-3,4-dihydro-quinazolin-2(1h)-one
반응식
[CH:1]([N:4]([C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[CH:9]=1)[C:5]([NH2:7])=[O:6])([CH3:3])[CH3:2].[CH2:17]1[O:21][C:20]2[CH:22]=[C:23]([Cl:28])[C:24]([CH:26]=O)=[CH:25][C:19]=2[O:18]1>>[CH:1]([N:4]1[C:8]2[C:13](=[CH:12][C:11]3[O:14][CH2:15][O:16][C:10]=3[CH:9]=2)[CH:26]([C:24]2[CH:25]=[C:19]3[O:18][CH2:17][O:21][C:20]3=[CH:22][C:23]=2[Cl:28])[NH:7][C:5]1=[O:6])([CH3:3])[CH3:2]참가 물질
3
실험 절차
This compound was synthesized from N-isopropyl-N-[3.4-(methylenedioxy)-phenyl]urea (410 mg) and 6-chloropiperonal (350 mg) by the procedure described in example 10 in 65% yield. 1H NMR (CDCl3): 6.86 (s, 1H), 6.77 (s, 1H), 6.48 (s, 1H), 6.40 (s, 1H), 5.95 (s, 4H), 5.66 (d, J=2.5, 1H), 5.21 (s, 1H), 4.48 (m, 1H), 1.53 (d, J=6.5, 6H).
출처 및 근거
- ORD 기록
- ord-0195ba5497f04fe6abe4c16bc9422980
- 출처 데이터셋
- uspto-grants-2004_07