p-Toluenesulfonic acid monohydrate → HCID 59815654, 화합물

HRID 2117363노트

반응식

HRID 2117363 반응식
[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]

참가 물질

7

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 598156466-(4-Benzyloxyphenylamino)-5-nitronicotinic acid methyl ester

생성물 1

HCID 59815654HCID 59815654, 화합물

시약·촉매·용매 4

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8857Ethyl Acetate용매HCID 9005Trimethyl orthoformate용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-ec24c21807e243308a1c4611c46985c5
출처 데이터셋
uspto-grants-2008_10
특허 번호
US07442709B2

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