5-Hydroxyoxindole → HCID 20540084, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[CH2:5]2.[C:12]1([S:18][CH2:19][CH2:20][CH2:21][CH2:22]Br)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[C:12]1([S:18][CH2:19][CH2:20][CH2:21][CH2:22][O:1][C:2]2[CH:3]=[C:4]3[C:8](=[CH:9][CH:10]=2)[NH:7][C:6](=[O:11])[CH2:5]3)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
3
Procedure
Prepared analogous to Example 140 from 5-hydroxy-oxindole (J. Chem. Soc. 1961, 2723) and 4-phenylmercapto- butyl bromide.
Sources & evidence
- ORD record
- ord-aa1ea26592e44a5ebfc04c4d3b1116bf
- Source dataset
- uspto-grants-1982_05
- Patent number
- US04329347
Reaction notes
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