Dichloromethane → HCID 68584049, compound

HRID 645992Notes

Reaction equation

HRID 645992 reaction equation
[CH:1]([N:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[N:6]([C:13]([NH:15][CH2:16][CH:17]2[CH2:22][CH2:21][N:20]([C:23]3([C:29]([O:31]C(C)(C)C)=[O:30])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]3)[CH2:19][CH2:18]2)=[O:14])[C:5]1=[O:36])([CH3:3])[CH3:2].FC(F)(F)C(O)=O.[Cl:44]CCl>>[ClH:44].[CH:1]([N:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[N:6]([C:13]([NH:15][CH2:16][CH:17]2[CH2:18][CH2:19][N:20]([C:23]3([C:29]([OH:31])=[O:30])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]3)[CH2:21][CH2:22]2)=[O:14])[C:5]1=[O:36])([CH3:3])[CH3:2]

Participants

4

Procedure

To a stirred solution of tert-butyl 1-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]cyclohexanecarboxylate (400 mg, 0.802 mmol) in dichloromethane (5 mL) was added trifluoroacetic acid (5 mL, 65.2 mmol) at room temperature. After 12 h, the volatile components were removed under reduced pressure. To the residue was added 4N HCl in dioxane (5.0 mL) was added and stirred for 10 min. Then, the volatile was removed under reduced pressure.

Workup

  1. customthe volatile components were removed under reduced pressure
  2. additionTo the residue was added 4N HCl in dioxane (5.0 mL)
  3. additionwas added
  4. customThen, the volatile was removed under reduced pressure

Sources & evidence

ORD record
ord-f94bc1576dcd4e138bc4481709106674
Source dataset
uspto-grants-2010_04
Patent number
US07705020B2

Reaction notes

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