Water → HCID 66978307, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[NH:12][C:11](=[O:13])[N:10]([CH:14]3[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)[CH2:9][CH2:8][C:7]=2[CH:20]=1.[Cl:21][C:22]1[C:30]2[N:29]=[C:28]([CH3:31])[NH:27][C:26]=2[CH:25]=[CH:24][C:23]=1[O:32][C:33]1[CH:38]=[C:37](Cl)[N:36]=[CH:35][N:34]=1.CCN(C(C)C)C(C)C.O>CN(C=O)C>[Cl:21][C:22]1[C:30]2[N:29]=[C:28]([CH3:31])[NH:27][C:26]=2[CH:25]=[CH:24][C:23]=1[O:32][C:33]1[N:34]=[CH:35][N:36]=[C:37]([N:17]2[CH2:18][CH2:19][CH:14]([N:10]3[CH2:9][CH2:8][C:7]4[CH:20]=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][C:6]=4[NH:12][C:11]3=[O:13])[CH2:15][CH2:16]2)[CH:38]=1Participants
6
Procedure
100 mg (0.36 mmol) 7-methoxy-3-piperidin-4-yl-1,3,4,5-tetrahydro-1,3-benzodiazepin-2-one, 110 mg (0.37 mmol) 4-chloro-5-(6-chloropyrimidin-4-yloxy)-2-methyl-1H-benzo[d]-imidazole and 0.14 mL (0.81 mmol) DIPEA in 2.0 mL DMF were stirred for 3 h at RT and for 4 h at 40° C. The reaction mixture was mixed with water. The precipitate formed was suction filtered, washed and dried. The filtrate was again suction filtered, washed and dried.
Workup
- customThe precipitate formed
- filtrationfiltered
- washwashed
- customdried
- filtrationfiltered
- washwashed
- customdried
Sources & evidence
- ORD record
- ord-ff52105de00747948fe720e7fa4264b6
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08952014B2
Reaction notes
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