Hydrochloric Acid → HCID 67455002, compound

HRID 2273860Notes

Reaction equation

HRID 2273860 reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([NH:11][C:12](=[O:26])[C:13]2[CH:18]=[CH:17][CH:16]=[N:15][C:14]=2[C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[CH:20]=2)[CH:8]=[CH:9][CH:10]=1)([CH3:4])([CH3:3])[CH3:2].Cl>[Pt]=O.C(O)C>[C:1]([C:5]1[CH:6]=[C:7]([NH:11][C:12]([CH:13]2[CH2:18][CH2:17][CH2:16][NH:15][CH:14]2[C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[CH:20]=2)=[O:26])[CH:8]=[CH:9][CH:10]=1)([CH3:4])([CH3:2])[CH3:3]

Participants

5

Procedure

A mixture of N-(3-tert-butylphenyl)-2-(3-fluorophenyl)nicotinamide (501.2 mg, 1.4 mmol), platinum oxide (51.9 mg, 0.21 mmol), and concentrated HCl (400 μL, 5.2 mmol) in 5 ml, of ethanol was stirred vigorously under hydrogen balloon overnight. The mixture was filtered, and the solids washed with 25 mL of methanol three times. The combined solution was dried under reduced pressure. To the residue was added 30 mL of saturated sodium bicarbonate and 150 mL of EtOAc. The organic layer was separated, and dried over sodium sulfate. Evaporation of solvent gave the crude 2-(3-fluorophenyl)piperidine-3-carboxylic acid (3-tert-butylphenyl)amide as a brown solid, which was taken on directly to the next step. MS: (ES) m/z 355.7 (M+H+).

Workup

  1. filtrationThe mixture was filtered
  2. washthe solids washed with 25 mL of methanol three times
  3. customThe combined solution was dried under reduced pressure
  4. additionTo the residue was added 30 mL of saturated sodium bicarbonate and 150 mL of EtOAc
  5. customThe organic layer was separated
  6. dry with materialdried over sodium sulfate
  7. customEvaporation of solvent

Sources & evidence

ORD record
ord-19b30578cd2e47a39b806726fbe88ba0
Source dataset
uspto-grants-2015_09
Patent number
US09126939B2

Reaction notes

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