5-Chloro-2-methyl-3-nitroaniline → HCID 18789611、化合物
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([O:14][CH2:15][C:16]2[NH:17][CH2:18][CH2:19][N:20]=2)[C:5]([CH3:13])=[C:6]([NH:8][S:9]([CH3:12])(=[O:11])=[O:10])[CH:7]=1.ClC1C=CC(NS(C)(=O)=O)=C(C)C=1OCC1NCCN=1.ClC1C=C([N+]([O-])=O)C(C)=C(C=1)N>>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([O:14][CH2:15][C:16]2[NH:20][CH2:19][CH2:18][N:17]=2)[C:5]([CH3:13])=[C:6]([NH:8][S:9]([CH3:12])(=[O:11])=[O:10])[CH:7]=1参加物
4
実験手順
N-[5-chloro-3-(4,5-dihydro-1H-imidazol-2-ylmethoxy)-2-methylphenyl]methane-sulfonamide, mp 198.1-199.3° C., was prepared in a similar manner to that described above for N-[4-chloro-3-(4,5-dihydro-1H-imidazol-2-ylmethoxy)-2-methylphenyl]methane-sulfonamide, except the starting material was 5-chloro-2-methyl-3-nitroaniline described in Scheme Q (Example 6D).
出典と根拠
- ORDレコード
- ord-001cbfe66a874040b590028a3bc22226
- 出典データセット
- uspto-grants-2000_05