Hydrochloric Acid → 6-[4-(Azetidin-3-yloxy)-3-methoxy-phenyl]-2-(4-chloro-phenyl)-5,6-dihydro-4H-thieno[2,3-c]pyridin-7-one hydrochloride

HRID 2384908Notes

Reaction equation

HRID 2384908 reaction equation
[NH:1]1[CH2:4][CH:3]([O:5][C:6]2[CH:11]=[CH:10][C:9]([N:12]3[CH2:17][CH2:16][C:15]4[CH:18]=[C:19]([C:21]5[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=5)[S:20][C:14]=4[C:13]3=[O:28])=[CH:8][C:7]=2[O:29][CH3:30])[CH2:2]1.Cl>C(Cl)Cl.C(O)C>[ClH:27].[NH:1]1[CH2:2][CH:3]([O:5][C:6]2[CH:11]=[CH:10][C:9]([N:12]3[CH2:17][CH2:16][C:15]4[CH:18]=[C:19]([C:21]5[CH:22]=[CH:23][C:24]([Cl:27])=[CH:25][CH:26]=5)[S:20][C:14]=4[C:13]3=[O:28])=[CH:8][C:7]=2[O:29][CH3:30])[CH2:4]1

Participants

5

Procedure

Prepare the HCl salt by dissolving the residue in CH2Cl2 and adding HCl in ethanol. Add ether to the mixture then filter and dry the solid to obtain the title compound. LC-MS/ES m/z (35Cl) 441.0 [M+H]+.

Workup

  1. filtrationAdd ether to the mixture then filter
  2. customdry the solid

Sources & evidence

ORD record
ord-9b44716eb4e94ac98a92731479aba650
Source dataset
uspto-grants-2012_09
Patent number
US08263772B2

Reaction notes

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