Dimethyl Sulfoxide → 4-[(3,4-Dimethylphenyl)(methyl)amino]-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinecarbaldehyde

HRID 572518노트

반응식

HRID 572518 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH3:11][C:12]1[CH:13]=[C:14]([N:19]([CH3:34])[C:20]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[C:23](=[O:30])[N:22]([CH3:31])[C:21]=2[CH2:32][OH:33])[CH:15]=[CH:16][C:17]=1[CH3:18].CCN(CC)CC>C(Cl)Cl>[CH3:11][C:12]1[CH:13]=[C:14]([N:19]([CH3:34])[C:20]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[C:23](=[O:30])[N:22]([CH3:31])[C:21]=2[CH:32]=[O:33])[CH:15]=[CH:16][C:17]=1[CH3:18]

참가 물질

6

실험 절차

To a solution of oxalyl chloride (0.015 mL, 0.172 mmol) in DCM (5 mL) at −70° C. was added dropwise DMSO (0.024 mL, 0.344 mmol). After 15 min a solution of 4-[(3,4-dimethylphenyl)(methyl)amino]-3-(hydroxymethyl)-2-methyl-1(2H)-isoquinolinone (25 mg, 0.078 mmol) in DCM (1 mL) was added slowly, and the mixture was kept at −78° C. for 30 min. Then NEt3 (38 uL) was added and the reaction was kept at −78° C. for 1 hour. The mixture was quenched with aq. NaHCO3 and extracted with dichloromethane. The organic phase was dried over sodium sulfate and evaporated to give the crude title compound as yellow oil (16.9 mg, 61.4%). 1H NMR (400 MHz, CDCl3) δ ppm 9.97-9.78 (m, 1 H), 8.64-8.46 (m, 1 H), 7.75-7.54 (m, 2 H), 7.51-7.42 (m, 1 H), 7.07-6.92 (m, 1 H), 6.59-6.38 (m, 2 H), 3.87 (s, 3 H), 3.40 (s, 3 H), 2.18 (d, J=6.3 Hz, 6 H); ES-LCMS: 321.1 (M+1).

후처리

  1. waitthe reaction was kept at −78° C. for 1 hour
  2. customThe mixture was quenched with aq. NaHCO3
  3. extractionextracted with dichloromethane
  4. dry with materialThe organic phase was dried over sodium sulfate
  5. customevaporated

출처 및 근거

ORD 기록
ord-4d06197666ce480fb8e6fc0c30fba5db
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09029391B2

반응 노트

불러오는 중…