Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4](/[CH:9]=[CH:10]/[C:11]([N:13]2[CH2:19][CH2:18][C:17](=[O:20])[NH:16][CH2:15][CH2:14]2)=[O:12])[CH:5]=[CH:6][C:7]=1[Cl:8].[Cl:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]I>>[Cl:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][N:16]1[C:17](=[O:20])[CH2:18][CH2:19][N:13]([C:11](=[O:12])/[CH:10]=[CH:9]/[C:4]2[CH:5]=[CH:6][C:7]([Cl:8])=[C:2]([Cl:1])[CH:3]=2)[CH2:14][CH2:15]1Participants
3
Procedure
In analogy to the procedure described in example 5A, 1-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-[1,4]diazepan-5-one (intermediate 1A]) and 1-chloro-5-iodopentane gave the title compound as yellow oil. MS: 416.9 (MH+, 3Cl).
Sources & evidence
- ORD record
- ord-9fc93f82fc164efa8468f64f82d0e3ad
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07632829B2
Linked notes
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