Ethyl bromoacetate → HCID 21104958, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:10]=[C:11]([S:22][CH2:23][C:24]3[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=3)[NH:12][C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)=[CH:5][CH:4]=1.Br[CH2:31][C:32]([O:34][CH2:35][CH3:36])=[O:33].[H-].[Na+]>>[CH3:21][O:20][C:17]1[CH:16]=[CH:15][C:14]([C:13]2[N:12]=[C:11]([S:22][CH2:23][C:24]3[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=3)[N:10]([CH2:31][C:32]([O:34][CH2:35][CH3:36])=[O:33])[C:9]=2[C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)=[CH:19][CH:18]=1Participants
4
Procedure
Starting substances: 500 mg (1.2 mmol) of T70 from Example 31; 270 mg (1.6 mmol) of ethyl bromoacetate; 72 mg (3 mmol) of NaH
Sources & evidence
- ORD record
- ord-0d13f24638db445c93c9f35b8f002155
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07223781B2
Reaction notes
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