Hydrochloric Acid → HCID 15985975, compound

HRID 1445484Notes

Reaction equation

HRID 1445484 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]=1

Participants

4

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

  1. customThe suspension is partly evaporated
  2. washThe product is washed with water and diisopropylether
  3. customdried in vacuo

Sources & evidence

ORD record
ord-65724db3e2414c34840c7ff0a8c2d742
Source dataset
uspto-grants-2010_02
Patent number
US07666868B2

Reaction notes

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