Potassium Hydroxide → HCID 21945946, compound

HRID 1295754Notes

Reaction equation

HRID 1295754 reaction equation
C[O:2][C:3]([C:5]1[C:6]([CH3:24])=[C:7]2[N:12]([CH:13]=1)[N:11]=[CH:10][N:9]=[C:8]2[CH:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[NH:16][C:15]1=[O:23])=[O:4].[OH-].[K+]>CO>[O:23]=[C:15]1[CH:14]([C:8]2[C:7]3=[C:6]([CH3:24])[C:5]([C:3]([OH:4])=[O:2])=[CH:13][N:12]3[N:11]=[CH:10][N:9]=2)[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[NH:16]1

Participants

4

Conditions

Temperature
60 °C

Procedure

To a solution of Example 77 (3.3 g, 10.2 mmol) in methanol (600 mL) was added potassium hydroxide (1N aqueous solution, 200 mL) and the mixture was deoxygenated by purging with argon. The reaction mixture was heated to 60° C. for 20 hrs. The reaction mixture was cooled and concentrated to about 50 mL and the residue was acidified with concentrated HCl to pH 4. The yellow solid was collected, washed with water, and dried in vacuo to afford the title compound (2.9 g, 92%). MS: [M+H]+=307.1; 1H NMR (CD3OD): δ 7.94 (s, 1H), 7.71 (s, 1H), 7.18-7.10 (m, 2H), 6.94-6.86 (m, 2H), 2.45 (s, 3H).

Workup

  1. customthe mixture was deoxygenated
  2. customby purging with argon
  3. temperatureThe reaction mixture was cooled
  4. concentrationconcentrated to about 50 mL
  5. customThe yellow solid was collected
  6. washwashed with water
  7. customdried in vacuo

Sources & evidence

ORD record
ord-dffbd07bf6fa44e6a28b430383d25fa6
Source dataset
uspto-grants-2007_07
Patent number
US07244733B2

Reaction notes

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