Hydrochloric Acid → HCID 15985975, compound
Reaction equation
[CH3:1][N:2]1[CH:6]=[C:5]([C:7]2[CH:8]=[C:9]([S:13]([N:16]3[CH:20]=[CH:19][C:18](/[CH:21]=[CH:22]/[C:23]([NH:25][O:26]C4CCCCO4)=[O:24])=[CH:17]3)(=[O:15])=[O:14])[CH:10]=[CH:11][CH:12]=2)[CH:4]=[N:3]1.Cl>CO>[OH:26][NH:25][C:23](=[O:24])/[CH:22]=[CH:21]/[C:18]1[CH:19]=[CH:20][N:16]([S:13]([C:9]2[CH:10]=[CH:11][CH:12]=[C:7]([C:5]3[CH:4]=[N:3][N:2]([CH3:1])[CH:6]=3)[CH:8]=2)(=[O:15])=[O:14])[CH:17]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 0.086 g (E)-3-{1-[3-(1-methyl-1H-pyrazol-4-yl)-benzenesulfonyl]-1H-pyrrol-3-yl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide with 3.0 ml methanol and 7.0 ml 1M aqueous HCl is stirred at ambient temperature for 24 h. The suspension is partly evaporated and the residual mixture is centrifuged. The product is washed with water and diisopropylether and dried in vacuo. By this method 0.045 g of a light pink powder are obtained. Melting point: 155-160° C., sinter is beginning from 85° C.
Workup
- customThe suspension is partly evaporated
- washThe product is washed with water and diisopropylether
- customdried in vacuo
Sources & evidence
- ORD record
- ord-65724db3e2414c34840c7ff0a8c2d742
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666868B2
Reaction notes
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