Ethyl indole-2-carboxylate → HCID 58900301, compound
Reaction equation
C([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:5])C.Br[CH2:16][C:17]1[C:18]2[CH:25]=[C:24]([Cl:26])[CH:23]=[CH:22][C:19]=2[S:20][CH:21]=1>>[Cl:26][C:24]1[CH:23]=[CH:22][C:19]2[S:20][CH:21]=[C:17]([CH2:16][N:7]3[C:8]4[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=4)[CH:14]=[C:6]3[C:4]([OH:3])=[O:5])[C:18]=2[CH:25]=1Participants
3
Procedure
Using general procedure B, 1H-indole-2-carboxylic acid ethyl ester was coupled with 3-bromomethyl-5-chloro-benzo[b]thiophene and the product obtained was hydrolyzed to give the title compound as a white solid. MS: 340.0 ([M−H]−).
Workup
- customthe product obtained
Sources & evidence
- ORD record
- ord-5a59a9f9e4284c6cb1ea3886360d3ed6
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696240B2
Reaction notes
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