2-Amino-1-(N-cyclopropylmethylamino)-4-(isopropylsulfonyl)benzene → 1-(Cyclopropylmethyl)-2-(1-methylcyclopentylmethyl)-5-(isopropylsulfonyl)-1H-benzimidazole
Reaction equation
[CH3:1][C:2]1([CH2:7][C:8](Cl)=O)[CH2:6][CH2:5][CH2:4][CH2:3]1.[NH2:11][C:12]1[CH:17]=[C:16]([S:18]([CH:21]([CH3:23])[CH3:22])(=[O:20])=[O:19])[CH:15]=[CH:14][C:13]=1[NH:24][CH2:25][CH:26]1[CH2:28][CH2:27]1>>[CH:26]1([CH2:25][N:24]2[C:13]3[CH:14]=[CH:15][C:16]([S:18]([CH:21]([CH3:23])[CH3:22])(=[O:20])=[O:19])=[CH:17][C:12]=3[N:11]=[C:8]2[CH2:7][C:2]2([CH3:1])[CH2:6][CH2:5][CH2:4][CH2:3]2)[CH2:27][CH2:28]1Participants
3
Procedure
The title compound was prepared according to the procedure described in Step C of Example 5 from (1-methylcyclopentyl)acetyl chloride (Step A) and 2-amino-1-(N-cyclopropylmethylamino)-4-(isopropylsulfonyl)benzene (Step E of Example 1).
Sources & evidence
- ORD record
- ord-23203796bfef493093ec4f231dd7f763
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07598393B2
Reaction notes
Loading…