Ethyl formimidate hydrochloride → 1-(Iminomethyl)piperidin-4-yl (2R)-2-((1R)-3,3-difluorocyclopentyl)-2-hydroxy-2-(4-bromophenyl)-ethanoate Monohydrochloride

HRID 1785252Notes

Reaction equation

HRID 1785252 reaction equation
[F:1][C:2]1([F:25])[CH2:6][CH2:5][C@@H:4]([C@@:7]([OH:24])([C:17]2[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][CH:18]=2)[C:8]([O:10][CH:11]2[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]2)=[O:9])[CH2:3]1.[ClH:26].[CH:27](=[NH:31])OCC>C(O)C>[ClH:26].[F:25][C:2]1([F:1])[CH2:6][CH2:5][C@@H:4]([C@@:7]([OH:24])([C:17]2[CH:18]=[CH:19][C:20]([Br:23])=[CH:21][CH:22]=2)[C:8]([O:10][CH:11]2[CH2:12][CH2:13][N:14]([CH:27]=[NH:31])[CH2:15][CH2:16]2)=[O:9])[CH2:3]1

Participants

4

Reactant 2

HCID 12578842Ethyl formimidate hydrochlorideHCID 69766871piperidin-4-yl (2R)-2-((1R)-3,3-difluorocyclopentyl)-2-hydroxy-2-(4-bromophenyl)ethanoate

Product 1

HCID 697673051-(Iminomethyl)piperidin-4-yl (2R)-2-((1R)-3,3-difluorocyclopentyl)-2-hydroxy-2-(4-bromophenyl)-ethanoate MonohydrochlorideYield 60.1%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a solution of 13 mg of piperidin-4-yl (2R)-2-((1R)-3,3-difluorocyclopentyl)-2-hydroxy-2-(4-bromophenyl)ethanoate in 1 ml of anhydrous ethanol, 4 mg of ethyl formimidate hydrochloride was added, followed by 13 hours' stirring at room temperature. The reaction liquid was condensed to dry solid. Purifying the crude product on silica gel column chromatography (eluent: chloroform/methanol=10/1), 9 mg of the title compound was obtained as a colorless solid.

Workup

  1. customThe reaction liquid
  2. customcondensed
  3. customto dry solid
  4. customPurifying the crude product on silica gel column chromatography (eluent: chloroform/methanol=10/1)

Sources & evidence

ORD record
ord-4318591769994b8d97748cc15b9048f3
Source dataset
uspto-grants-2009_03
Patent number
US07504432B2

Reaction notes

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