Dichloromethane → HCID 68584049, compound

HRID 16606Notes

Reaction equation

HRID 16606 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

Reactant 3

HCID 6344DichloromethaneHCID 6422Trifluoroacetic acidHCID 68585066HCID 68585066, compound

Product 1

HCID 68584049HCID 68584049, compound

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-a80ac923e2924e87861b55551440b073
Source dataset
uspto-grants-2010_06
Patent number
US07737163B2

Reaction notes

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