Ethanethiol → HCID 21702000, compound
Reaction equation
C[O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:10]([C:11]([C:13]3[CH:18]=[CH:17][C:16]([O:19][CH2:20][CH:21]([O:30]C)[CH2:22][NH:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28]C)=[CH:15][CH:14]=3)=[O:12])=[C:9]([C:32]3[CH:37]=[CH:36][C:35]([O:38]C)=[CH:34][CH:33]=3)[S:8][C:7]=2[CH:40]=1.C(S)C.[Cl-].[Al+3].[Cl-].[Cl-]>>[OH:2][C:3]1[CH:4]=[CH:5][C:6]2[C:10]([C:11]([C:13]3[CH:14]=[CH:15][C:16]([O:19][CH2:20][CH:21]([OH:30])[CH2:22][NH:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH:17][CH:18]=3)=[O:12])=[C:9]([C:32]3[CH:33]=[CH:34][C:35]([OH:38])=[CH:36][CH:37]=3)[S:8][C:7]=2[CH:40]=1Participants
4
Procedure
[6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl][4-(2-methoxy-3-hexylaminopropoxy)phenyl]methanone (340 mg, 0.62 mmol) was converted to 200 mg of the title compound by the procedure of Example 32 using 0.23 mL (3.1 mmol) of ethanethiol 660 mg (5.0 mmol) of aluminum chloride.
Sources & evidence
- ORD record
- ord-213f4c1260da491e98f78f4a22e4ff35
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06090843
Reaction notes
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