Tetrahydrofuran → HCID 22346671, compound

HRID 897749Notes

Reaction equation

HRID 897749 reaction equation
[BH4-].[Na+].[NH2:3][C:4]1[N:9]=[CH:8][N:7]=[C:6]2[N:10]([C:26]3[CH:33]=[CH:32][C:29]([CH:30]=[O:31])=[CH:28][CH:27]=3)[N:11]=[C:12]([C:13]3[CH:18]=[CH:17][C:16]([O:19][C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)=[CH:15][CH:14]=3)[C:5]=12.C1COCC1>CO>[NH2:3][C:4]1[N:9]=[CH:8][N:7]=[C:6]2[N:10]([C:26]3[CH:27]=[CH:28][C:29]([CH2:30][OH:31])=[CH:32][CH:33]=3)[N:11]=[C:12]([C:13]3[CH:14]=[CH:15][C:16]([O:19][C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)=[CH:17][CH:18]=3)[C:5]=12

Participants

5

Procedure

Sodium borohydride (19 mg, 0.491 mmol) was added to a solution of 4-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]benzaldehyde (100 mg, 0.245 mmol) in methanol (2 mL). After 16 hours, THF (1 mL) and more sodium borohydride (19 mg, 0.491 mmol) was added. 5 hours later, the solvent was removed and water was added. The aqueous layer was extracted with dichloromathane. The combined organic layer was washed with brine, dried over MgSO4, filtered and evaporated. The residue was purified by flash column chromatography using ethyl acetate/dichloromethane (80:20 to 100:0) as mobile phase to give {4-[4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]phenyl}methanol (36 mg, 36%).

Workup

  1. custom5 hours later, the solvent was removed
  2. additionwater was added
  3. extractionThe aqueous layer was extracted with dichloromathane
  4. washThe combined organic layer was washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue was purified by flash column chromatography

Sources & evidence

ORD record
ord-579bb5a02d63454f8238acfe675774dc
Source dataset
uspto-grants-2005_07
Patent number
US06921763B2

Reaction notes

Loading…