Dimethylamine → HCID 86584775, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9](=[O:24])[N:10]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH2:19][CH2:20][CH2:21][CH2:22]Br)=[CH:14][CH:13]=2)[CH3:11])=[CH:4][CH:3]=1.[CH3:25][NH:26][CH3:27]>>[CH:9]([OH:24])=[O:8].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9](=[O:24])[N:10]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH2:19][CH2:20][CH2:21][CH2:22][N:26]([CH3:27])[CH3:25])=[CH:14][CH:13]=2)[CH3:11])=[CH:4][CH:3]=1Participants
3
Procedure
In analogy to example 17.1, reaction of [4-(4-Bromo-butoxy)-phenyl]-methyl-carbamic acid 4-chloro-phenyl ester with 10 eq dimethylamine (33% in ethanol, 5.6 M) yielded [4-(4-Dimethylamino-butoxy)-phenyl]-methyl-carbamic acid 4-chloro-phenyl ester; compound with formic acid, MS: 377 (MH+).
Sources & evidence
- ORD record
- ord-7bee95063ef74effb25b8c4d16789881
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06683201B2
Reaction notes
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