Benzo(B)Thiophene → HCID 19846308, compound
Reaction equation
[OH:1][N:2]([CH:6](C1SC2C=CC(CC(C)C)=CC=2C=1)[CH3:7])[C:3]([NH2:5])=[O:4].[S:21]1[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[CH:23]=[CH:22]1>>[OH:1][N:2]([CH:6]([C:23]1[C:24]2[CH:29]=[C:28]([CH2:23][CH:24]([CH3:29])[CH3:25])[CH:27]=[CH:26][C:25]=2[S:21][CH:22]=1)[CH3:7])[C:3]([NH2:5])=[O:4]Participants
3
Procedure
N-hydroxy-N-[1-(5-(2,2-dimethylethyl)benzo[b]thien-2-yl)-ethyl]urea. The desired compound was prepared according to the method of example 2, except using the material prepared as in step c, above, instead of benzothiophene. (R1 =NH2, A=CHCH3, X=S[2-isomer], Y=5-(CH3)3C).
Workup
- customthe material prepared as in step c
Sources & evidence
- ORD record
- ord-527a2e6ccd4b49a59b918032d29d5c6a
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04873259
Reaction notes
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