HCID 18452906, compound → 2-Mercaptobenzonitrile
Reaction equation
[S:1](O)(=O)(=O)[CH3:2].[CH2:6]1[CH:15]2C([CH2:11][CH2:12][CH2:13][CH2:14]2)CC[NH:7]1>CC(C)=O.C(=O)([O-])[O-].[K+].[K+]>[SH:1][C:2]1[CH:11]=[CH:12][CH:13]=[CH:14][C:15]=1[C:6]#[N:7]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Following the procedures for Example 22, Step C, decahydroisoquinoline mesylate from preparation 3 (102 mg, 0.28 mmol) in acetone (0.5 mL), potassium carbonate solid (38 mg, 0.28 mmol, twice) and 2-mercaptobenzonitrile (38 mg, 0.286 mmol, twice) gave, after flash chromatography (hexanes-ethyl acetate 2:1), the desired product as an oil (64 mg) in 57% yield.
Sources & evidence
- ORD record
- ord-33b0a434132040a9891258e8b1995164
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07205313B2
Reaction notes
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