Lithium Hydroxide → 3-[({[1,6-Diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}amino)carbonyl]benzoic Acid

HRID 564551Notes

Reaction equation

HRID 564551 reaction equation
[CH2:1]([N:3]1[C:7]2=[N:8][C:9]([CH2:33][CH3:34])=[C:10]([CH2:19][NH:20][C:21]([C:23]3[CH:24]=[C:25]([CH:30]=[CH:31][CH:32]=3)[C:26]([O:28]C)=[O:27])=[O:22])[C:11]([NH:12][CH:13]3[CH2:18][CH2:17][O:16][CH2:15][CH2:14]3)=[C:6]2[CH:5]=[N:4]1)[CH3:2].[Li+].[OH-]>CO.O>[CH2:1]([N:3]1[C:7]2=[N:8][C:9]([CH2:33][CH3:34])=[C:10]([CH2:19][NH:20][C:21]([C:23]3[CH:24]=[C:25]([CH:30]=[CH:31][CH:32]=3)[C:26]([OH:28])=[O:27])=[O:22])[C:11]([NH:12][CH:13]3[CH2:18][CH2:17][O:16][CH2:15][CH2:14]3)=[C:6]2[CH:5]=[N:4]1)[CH3:2]

Participants

5

Conditions

Temperature
80 °C

Procedure

To a solution of methyl 3-[({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}amino)carbonyl]benzoate (705 mg, 1.514 mmol) in MeOH (4.5 mL) and H2O (2.250 mL) was added LiOH (181 mg, 7.57 mmol). This mixture was heated in a microwave at 80° C. for 30 min. The reaction mixture was concentrated, acidified with HCl to ph ˜5, filtered, and washed with MeOH/H2O (20%) to afford 0.5813 g (85%) of the title compound. LC-MS m/z 452 (M+H)+.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. filtrationfiltered
  3. washwashed with MeOH/H2O (20%)

Sources & evidence

ORD record
ord-beff84b1c64f4d9091a970c8d50fd004
Source dataset
uspto-grants-2011_11
Patent number
US08067408B2

Reaction notes

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