1-Acetoxy-2-bromoethane → HCID 70277252, compound
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][C:11]2[CH:20]=[C:19]([CH3:21])[C:18]3[C:13](=[CH:14][C:15]([NH:22][S:23]([C:26]4[CH:27]=[CH:28][CH:29]=[C:30]5[C:35]=4[N:34]=[CH:33][CH:32]=[CH:31]5)(=[O:25])=[O:24])=[CH:16][CH:17]=3)[N:12]=2)=[CH:5][CH:4]=1)#[N:2].[C:36]([O:39][CH2:40][CH2:41]Br)(=[O:38])[CH3:37]>>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][C:11]2[CH:20]=[C:19]([CH3:21])[C:18]3[C:13](=[CH:14][C:15]([N:22]([S:23]([C:26]4[CH:27]=[CH:28][CH:29]=[C:30]5[C:35]=4[N:34]=[CH:33][CH:32]=[CH:31]5)(=[O:25])=[O:24])[CH2:37][C:36]([O:39][CH2:40][CH3:41])=[O:38])=[CH:16][CH:17]=3)[N:12]=2)=[CH:5][CH:4]=1)#[N:2]Participants
3
Procedure
Prepared analogously to Example 1d from 2-[(4-cyanophenyl)-oxymethyl]-4-methyl-7-(quinoline-8-sulphonylamino)-quinoline and bromoethyl acetate.
Sources & evidence
- ORD record
- ord-4d31c15fb53049cdbfd6eba641fb9a2e
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121308
Reaction notes
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