4-(Chloromethyl)benzoic acid → 4-Chloromethyl-N-(7-[1,4]dioxepan-6-yl-4-methoxy-benzothiazol-2-yl)-benzamide
Reaction equation
[O:1]1[CH2:7][CH:6]([C:8]2[C:16]3[S:15][C:14]([NH2:17])=[N:13][C:12]=3[C:11]([O:18][CH3:19])=[CH:10][CH:9]=2)[CH2:5][O:4][CH2:3][CH2:2]1.[Cl:20][CH2:21][C:22]1[CH:30]=[CH:29][C:25]([C:26](O)=[O:27])=[CH:24][CH:23]=1.O1CC(C2C3SC(NC(C4SC(C)=CC=4)=O)=NC=3C(OC)=CC=2)COCC1>>[Cl:20][CH2:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([NH:17][C:14]2[S:15][C:16]3[C:8]([CH:6]4[CH2:5][O:4][CH2:3][CH2:2][O:1][CH2:7]4)=[CH:9][CH:10]=[C:11]([O:18][CH3:19])[C:12]=3[N:13]=2)=[O:27])=[CH:24][CH:23]=1Participants
4
Reactant 3
Product 1
Procedure
Using 7-[1,4]dioxepan-6-yl-4-methoxy-benzothiazol-2-ylamine and 4-chloromethyl-benzoic acid, the title compound was prepared in the same manner as described for 5-methyl-thiophene-2-carboxylic acid (7-[1,4]dioxepan-6-yl-4-methoxy-benzothiazol-2-yl)-amide and obtained as light brown powder. MS: m/e=434(M+H+).
Workup
- customobtained as light brown powder
Sources & evidence
- ORD record
- ord-01cb9a7247c4447581001e81591105b2
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07371748B2
Reaction notes
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