p-Toluenesulfonic acid monohydrate → HCID 59815654, compound

HRID 2117363Notes

Reaction equation

HRID 2117363 reaction equation
[CH3:1][O:2][C:3](=[O:28])[C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[C:7]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([O:20]CC3C=CC=CC=3)=[CH:16][CH:15]=2)=[N:6][CH:5]=1.O.[C:30]1(C)C=CC(S(O)(=O)=O)=CC=1>CO.C(OCC)(=O)C.C(OC)(OC)OC.[Pd]>[CH3:1][O:2][C:3]([C:4]1[CH:9]=[C:8]2[N:10]=[CH:30][N:13]([C:14]3[CH:15]=[CH:16][C:17]([OH:20])=[CH:18][CH:19]=3)[C:7]2=[N:6][CH:5]=1)=[O:28]

Participants

7

Procedure

To a suspension of XXIV (235 mg, 0.62 mmol) in MeOH (3 mL) and ethyl acetate (3 mL) was added 10% Pd—C (47 mg) under nitrogen atmosphere. The resulting mixture was hydrogenated at rt overnight. The catalyst was removed by filtration under nitrogen and washed with methanol, the filtrate was concentrated under reduced pressure to give a white solid. MS (ES, Pos.): m/z 260 [MH+]. The hydrogenation product was suspended in trimethyl orthoformate (5 mL), and p-toluenesulfonic acid monohydrate (12 mg, 0.062 mmol) was added. The resulting mixture was stirred at rt overnight. The white solid was collected by filtration. MS (ES, Pos.): m/z 270 [MH+]. 1H NMR (CD3OD, 400 MHz): δ=3.99 (s, 3H), 7.00 (d, J=8.8 Hz, 2H), 7.59 (d, J=8.8 Hz, 2H), 8.71 (d, J=1.8 Hz, 1H), 8.72 (s, 1H), 9.05 (d, J=1.8 Hz, 1H).

Workup

  1. customThe catalyst was removed by filtration under nitrogen
  2. washwashed with methanol
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customto give a white solid
  5. filtrationThe white solid was collected by filtration

Sources & evidence

ORD record
ord-ec24c21807e243308a1c4611c46985c5
Source dataset
uspto-grants-2008_10
Patent number
US07442709B2

Reaction notes

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