Water → HCID 67094378, compound
Reaction equation
Br[CH2:2][C:3]1[C:4]2[CH:19]=[C:18]([O:20][CH3:21])[C:17]([O:22][CH3:23])=[CH:16][C:5]=2[S:6][C:7]=1[C:8]([N:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1)=[O:9].[Cu][C:25]#[N:26].O>CN(C)C=O>[CH3:21][O:20][C:18]1[C:17]([O:22][CH3:23])=[CH:16][C:5]2[S:6][C:7]([C:8]([N:10]3[CH2:15][CH2:14][O:13][CH2:12][CH2:11]3)=[O:9])=[C:3]([CH3:2])[C:4]=2[C:19]=1[C:25]#[N:26]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
(4-Bromo-5,6-dimethoxy-3-methyl-benzo[b]thiophen-2-yl)-morpholin-4-yl-methanone (0.42 g) from Example 33 and copper(I) cyanide (2.0 g) in N,N-dimethylformamide (8 ml) were irradiated in a microwave oven at 150° C. for 1.5 hours. To the mixture water was added and the product was extracted into ethyl acetate. Ethyl acetate was dried and evaporated to dryness.
Workup
- extractionthe product was extracted into ethyl acetate
- dry with materialEthyl acetate was dried
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-20a112c1eef5458a83f1c3c6c804e4a0
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318785B2
Reaction notes
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