Oxalic Acid → HCID 86757083, compound

HRID 1070320Notes

Reaction equation

HRID 1070320 reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[OH:7][C:8]1[CH:9]=[CH:10][C:11]2[C:15]([CH2:16][C:17]3[CH:22]=[CH:21][C:20]([O:23][C@@H:24]4[CH2:29][CH2:28][CH2:27][CH2:26][C@H:25]4[N:30]4[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31]4)=[CH:19][CH:18]=3)=[C:14]([C:36]3[CH:41]=[CH:40][C:39]([O:42][CH2:43][CH2:44][N:45]4[CH2:49][CH2:48][CH2:47][CH2:46]4)=[CH:38][CH:37]=3)[S:13][C:12]=2[CH:50]=1>C(Cl)(Cl)Cl.CCOC(C)=O.C(Cl)(Cl)Cl>[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[OH:7][C:8]1[CH:9]=[CH:10][C:11]2[C:15]([CH2:16][C:17]3[CH:22]=[CH:21][C:20]([O:23][C@@H:24]4[CH2:29][CH2:28][CH2:27][CH2:26][C@H:25]4[N:30]4[CH2:31][CH2:32][CH2:33][CH2:34][CH2:35]4)=[CH:19][CH:18]=3)=[C:14]([C:36]3[CH:37]=[CH:38][C:39]([O:42][CH2:43][CH2:44][N:45]4[CH2:46][CH2:47][CH2:48][CH2:49]4)=[CH:40][CH:41]=3)[S:13][C:12]=2[CH:50]=1

Participants

5

Procedure

In approximately 4 mL of CHCl3-EtOAc (1:1) was dissolved 14.7 mg (0.164 mmol) of oxalic acid. To this was added dropwise 50.0 mg (0.082 mmol) of (±)-6-hydroxy-3-[4-[[trans-2-(1-piperidyl)cyclohexyl]oxy]benzyl]-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophene (Part C) in 7 mL of CHCl3. A white precipitate was formed, and the slurry was sonicated for 30 min and filtered with EtOAc rinse. The precipitate was dried over P2O5 at 55° C. in a vacuum oven.

Workup

  1. customA white precipitate was formed
  2. customthe slurry was sonicated for 30 min
  3. filtrationfiltered with EtOAc
  4. washrinse
  5. dry with materialThe precipitate was dried over P2O5 at 55° C. in a vacuum oven

Sources & evidence

ORD record
ord-8cc72c688c7b47b783b4e25ae5a6ae30
Source dataset
uspto-grants-2001_06
Patent number
US06251921B1

Reaction notes

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