Hydrochloric Acid → N-(azetidin-1-ylsulfonyl)-5-cyclopropyl-2-fluoro-4-((1-(trifluoromethyl)-cyclopentyl)methoxy)benzamide

HRID 1849600Notes

Reaction equation

HRID 1849600 reaction equation
[N:1]1([S:5]([NH:8][C:9](=[O:29])[C:10]2[CH:15]=[C:14](Cl)[C:13]([O:17][CH2:18][C:19]3([C:24]([F:27])([F:26])[F:25])[CH2:23][CH2:22][CH2:21][CH2:20]3)=[CH:12][C:11]=2[F:28])(=[O:7])=[O:6])[CH2:4][CH2:3][CH2:2]1.[CH:30]1(B(O)O)[CH2:32][CH2:31]1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].F[B-](F)(F)F.C1(P(C2CCCCC2)C2CCCCC2)CCCCC1.Cl>C1(C)C=CC=CC=1.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[N:1]1([S:5]([NH:8][C:9](=[O:29])[C:10]2[CH:15]=[C:14]([CH:30]3[CH2:32][CH2:31]3)[C:13]([O:17][CH2:18][C:19]3([C:24]([F:27])([F:26])[F:25])[CH2:23][CH2:22][CH2:21][CH2:20]3)=[CH:12][C:11]=2[F:28])(=[O:7])=[O:6])[CH2:4][CH2:3][CH2:2]1

Participants

9

Reactant 5

HCID 313Hydrochloric AcidHCID 62657Potassium Phosphate, TribasicHCID 2760897Cyclopropylboronic acidHCID 20066521Tri(cyclohexyl)phosphine tetrafluoroborateHCID 86703454N-(azetidin-1-ylsulfonyl)-5-chloro-2-fluoro-4-((1-(trifluoromethyl)-cyclopentyl)methoxy)benzamide

Product 1

HCID 86703455N-(azetidin-1-ylsulfonyl)-5-cyclopropyl-2-fluoro-4-((1-(trifluoromethyl)-cyclopentyl)methoxy)benzamideYield 61%

Reagents, catalysts & solvents 3

HCID 167845palladium(II) acetateCatalystHCID 962WaterSolventHCID 1140TolueneSolvent

Conditions

Temperature
100 °C

Procedure

To a mixture of N-(azetidin-1-ylsulfonyl)-5-chloro-2-fluoro-4-((1-(trifluoromethyl)-cyclopentyl)methoxy)benzamide (0.18 g, 0.39 mmol), cyclopropylboronic acid (0.40 g, 4.65 mmol) and potassium phosphate (2.55 g, 12.00 mmol) in toluene (20 mL) and water (1.0 mL) was sparged with a nitrogen atmosphere for 10 minutes, tricyclohexylphosphine tetrafluoroborate (0.17 g, 0.48 mmol) and palladium acetate (0.05 g, 0.22 mmol) was added to this reaction mixture. The reaction mixture was heated to 100° C. for 96 hours under a nitrogen atmosphere and then cooled to ambient temperature. 5% aqueous hydrochloric acid (20 mL) was added and the mixture was extracted with ethyl acetate (100 mL×3), the combined organics were washed with brine; dried over anhydrous sodium sulfate and concentrated in vacuo. Purification of the residue by column chromatography (10% to 30% gradient ethyl acetate in hexanes) afforded the title compound (0.11 g, 61%) as a colorless solid: 1H NMR (300 MHz, CDCl3) δ 8.63 (d, J=16.2 Hz, 1H), 7.62 (d, J=9.0 Hz, 1H), 6.57 (d, J=14.1 Hz, 1H), 4.23 (t, J=7.5 Hz, 4H), 3.99 (s, 2H), 2.31-2.20 (m, 2H), 2.08-1.94 (m, 3H), 1.89-1.70 (m, 6H), 0.95-0.88 (m, 2H), 0.67-0.60 (m, 2H); MS (ES+) m/z 465.1 (M+1), MS (ES−) m/z 463.1 (M−1).

Workup

  1. customwas sparged with a nitrogen atmosphere for 10 minutes
  2. temperaturecooled to ambient temperature
  3. extractionthe mixture was extracted with ethyl acetate (100 mL×3)
  4. washthe combined organics were washed with brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customPurification of the residue by column chromatography (10% to 30% gradient ethyl acetate in hexanes)

Sources & evidence

ORD record
ord-893782fbdf084b4bba2f612298247e1d
Source dataset
uspto-grants-2015_02
Patent number
US08952169B2

Reaction notes

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