Hydrochloric Acid → HCID 71599697, compound

HRID 926712Notes

Reaction equation

HRID 926712 reaction equation
Cl.C(OC([NH:9][C:10]1([C:40]([O:42][CH3:43])=[O:41])[CH2:15][CH2:14][N:13]([C:16]([C:18]2[CH:19]=[N:20][N:21]3[CH:26]=[CH:25][C:24]([N:27]4[CH2:31][CH2:30][CH2:29][C@@H:28]4[C:32]4[CH:37]=[C:36]([F:38])[CH:35]=[CH:34][C:33]=4[F:39])=[CH:23][C:22]=23)=[O:17])[CH2:12][CH2:11]1)=O)(C)(C)C>O1CCOCC1.O>[NH2:9][C:10]1([C:40]([O:42][CH3:43])=[O:41])[CH2:11][CH2:12][N:13]([C:16]([C:18]2[CH:19]=[N:20][N:21]3[CH:26]=[CH:25][C:24]([N:27]4[CH2:31][CH2:30][CH2:29][C@@H:28]4[C:32]4[CH:37]=[C:36]([F:38])[CH:35]=[CH:34][C:33]=4[F:39])=[CH:23][C:22]=23)=[O:17])[CH2:14][CH2:15]1

Participants

5

Conditions

Temperature
27.5 °C

Procedure

A mixture of 4M HCl solution in Dioxane (1 mL) and (R)-methyl 4-((tert-butoxycarbonyl)amino)-1-(5-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyridine-3-carbonyl)piperidine-4-carboxylate (50 g, 0.085 mmol) was stirred at 20-35° C. for 3 h. After which the reaction mixture was concentrated under reduced pressure to afford the crude. The residue obtained was dissolved in water, extracted with ethylacetate, washed with saturated NaHCO3 solution followed by brine and dried over anhydrous sodium sulfate, concentrated under reduced pressure to afford 15 mg of the title compound.

Workup

  1. concentrationAfter which the reaction mixture was concentrated under reduced pressure
  2. customto afford the crude
  3. customThe residue obtained
  4. extractionextracted with ethylacetate
  5. washwashed with saturated NaHCO3 solution
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-2b6c01001a9e4b289334d7f5663ebc65
Source dataset
uspto-grants-2016_03
Patent number
US09289419B2

Reaction notes

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