Hydrochloric Acid → HCID 11535873, compound

HRID 2405968Notes

Reaction equation

HRID 2405968 reaction equation
C(OC(=O)[NH:7][CH:8]1[CH2:13][CH2:12][N:11]([C:14]2[N:19]=[CH:18][N:17]=[C:16]3[NH:20][N:21]=[CH:22][C:15]=23)[CH2:10][CH2:9]1)(C)(C)C.Cl>C(OCC)C>[NH:20]1[C:16]2=[N:17][CH:18]=[N:19][C:14]([N:11]3[CH2:12][CH2:13][CH:8]([NH2:7])[CH2:9][CH2:10]3)=[C:15]2[CH:22]=[N:21]1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 24828862HCID 24828862, compound

Product 1

HCID 11535873HCID 11535873, compoundYield 177%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

To [1-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)-piperidin-4-yl]-carbamic acid tert-butyl ester (28 mg, 0.088 mmol) was added HCl (1 ml, 4M solution in dioxane, 4 mmol). The suspension was stirred at room temperature for 1 hour, and then diluted with diethyl ether (4 ml). The ethereal layer was discarded and the solid washed with a further portion of diethyl ether (2 ml). The ethereal layer was again discarded, and the resultant solid dried under high vacuum to yield the desired product (34 mg). The free base was liberated by dissolution of this material in methanol, loading onto an acidic resin SCX-2 cartridge, and elution from the cartridge with ammonia in methanol. LC/MS Rt 0.86 [M+H]+ 219

Workup

  1. washthe solid washed with a further portion of diethyl ether (2 ml)
  2. customthe resultant solid dried under high vacuum

Sources & evidence

ORD record
ord-778683b8640d467eb5107842001927e0
Source dataset
uspto-grants-2014_08
Patent number
US08809336B2

Reaction notes

Loading…