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Cyclohexyl bromide → {5-[(Cyclohexyl)-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester

HRID 15552
Notes
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Reaction equation

HRID 15552 reaction equation
[CH:1]1(Br)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C([O-])([O-])=O.[K+].[K+].[C:14]([O:18][C:19](=[O:44])[CH2:20][N:21]1[C:25]2[CH:26]=[CH:27][C:28]([NH:30][S:31]([C:34]3[CH:39]=[CH:38][C:37]([F:40])=[CH:36][CH:35]=3)(=[O:33])=[O:32])=[CH:29][C:24]=2[N:23]=[C:22]1[CH2:41][CH2:42][CH3:43])([CH3:17])([CH3:16])[CH3:15]>CC#N.CCOC(C)=O.O>[C:14]([O:18][C:19](=[O:44])[CH2:20][N:21]1[C:25]2[CH:26]=[CH:27][C:28]([N:30]([CH:1]3[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]3)[S:31]([C:34]3[CH:35]=[CH:36][C:37]([F:40])=[CH:38][CH:39]=3)(=[O:32])=[O:33])=[CH:29][C:24]=2[N:23]=[C:22]1[CH2:41][CH2:42][CH3:43])([CH3:17])([CH3:16])[CH3:15]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 7960Cyclohexyl bromideHCID 11430Potassium CarbonateHCID 67201670[5-(4-Fluoro-benzenesulfonylamino)-2-propyl-benzoimidazol-1-yl]-acetic acid tert-butyl ester

Product 1

HCID 67199864{5-[(Cyclohexyl)-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester

Reagents, catalysts & solvents 3

HCID 962
Water
Solvent
HCID 6342AcetonitrileSolvent
HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
80 °C

Procedure

Cyclohexyl bromide (0.27 mmol) and K2CO3 (63 mg, 0.45 mmol) were added to a solution of [5-(4-fluoro-benzenesulfonylamino)-2-propyl-benzoimidazol-1-yl]-acetic acid tert-butyl ester (40 mg, 0.09 mmol) in CH3CN (1 mL), and stirred overnight at 80° C. The reaction mixture was diluted with EtOAc and H2O, and then filtered through an Extrelut column. The column was washed with EtOAc, and the filtrate was concentrated. The crude product was carried onto the next reaction without any further purification or characterization.

Workup

  1. filtrationfiltered through an Extrelut column
  2. washThe column was washed with EtOAc
  3. concentrationthe filtrate was concentrated
  4. customThe crude product was carried onto the next reaction without any further purification or characterization

Sources & evidence

ORD record
ord-b83b3ed8d3fb450bb72195da87993890
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07732618B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes