Hydrochloric Acid → HCID 178418912, compound

HRID 133151Notes

Reaction equation

HRID 133151 reaction equation
C[O:2][C:3]([C:5]1[CH:6]=[C:7]([NH:10][C:11]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[N:14]=[C:13]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[N:12]=2)[NH:8][N:9]=1)=[O:4].[OH-].[Na+].Cl>>[C:3]([C:5]1[CH:6]=[C:7]([NH:10][C:11]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[N:14]=[C:13]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[N:12]=2)[NH:8][N:9]=1)([OH:4])=[O:2]

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 178418998HCID 178418998, compound

Product 1

HCID 178418912HCID 178418912, compoundYield 94.2%

Conditions

Temperature
50 °C

Procedure

(5-Methoxycarbonyl-2H-pyrazol-3-yl)-(2-phenyl-quinazolin-4-yl)-amine (III-73) (345 mg, 1 mmole in THF, 6 mL) was treated with NaOH (1M, 4.0 mL), stirred at 50° C. for 5 hours, cooled to room temperature, and neutralised with 1M HCl. The mixture was concentrated in vacuo to remove THF then diluted with water and the resulting precipitate filtered. The residual solid was dried at 80° C. under vacuum to afford III-72 as an off-white solid (312 mg, 94%): mp 289–291° C. (dec.); 1H NMR (DMSO) δ 7.45 (1H, br s), 7.50–7.60 (5H, m), 7.80–7.88 (2H, m), 7.40–7.50 (2H, m), 8.60–8.70 (1H, d), 10.70 (1H, s), 13.00–13.80 (2H, br s); IR (solid) 1699, 1624, 1607, 1570, 1539, 1506, 1486, 1398, 1333, 1256, 1177, 1004, 827, 764, 705; MS 332.3(M+H)+.

Workup

  1. temperaturecooled to room temperature
  2. concentrationThe mixture was concentrated in vacuo
  3. customto remove THF
  4. additionthen diluted with water
  5. filtrationthe resulting precipitate filtered
  6. customThe residual solid was dried at 80° C. under vacuum

Sources & evidence

ORD record
ord-e79ad2a2a272404f86ced0a2db3754e0
Source dataset
uspto-grants-2008_06
Patent number
US07390815B2

Reaction notes

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