Hydrochloric Acid → HCID 68295566, 화합물
반응식
[CH3:1][C:2]1[CH:24]=[C:23]([CH3:25])[CH:22]=[CH:21][C:3]=1[C:4]([C:6]1[CH:20]=[CH:19][CH:18]=[CH:17][C:7]=1[C:8]([N:10]([CH2:12][C:13]([O:15][CH3:16])=[O:14])[CH3:11])=[O:9])=O.C[O-].[Na+].Cl.CC1C=CC(S(O)(=O)=O)=CC=1>CO.C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH:24]=[C:23]([CH3:25])[CH:22]=[CH:21][C:3]=1[C:4]1[C:6]2[C:7](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:8](=[O:9])[N:10]([CH3:11])[C:12]=1[C:13]([O:15][CH3:16])=[O:14]참가 물질
실험 절차
An ice cold mixture of methyl 2-(2-(2,4-dimethylbenzoyl)-N-methylbenzamido)acetate (60 g, 177 mmol) in methanol (400 mL) was treated with sodium methoxide (42.0 g, 194 mmol) and the resultant was allowed to stir at ambient temperature for 1 hour. The mixture was cooled to 0° C., treated with HCl (21.78 mL, 265 mmol) and then concentrated. The residue was dissolved in ethyl acetate, washed with water, brine, dried over Na2SO4, filtered and concentrated. The crude intermediate was treated with Toluene (400 mL) and pTsOH (16.81 g, 88 mmol) and the mixture was heated at 120° C. for 1 hour. Additional pTsOH (16.81 g, 88 mmol) was added and the mixture was stirred at 120° C. overnight. LCMS indicated complete reaction. The mixture was concentrated and the residue was dissolved in ethyl acetate. The organic phase was washed with water, then brine, dried over Na2SO4, filtered and concentrated. The residue was purified on silica gel (0-60% EA on hexane) to give the desired product as a white solid (24 g, 53%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.48-8.57 (m, 1 H) 7.50-7.58 (m, 2 H) 7.10-7.14 (m, 1 H) 7.04 (s, 3 H) 3.61 (s, 3 H) 3.54 (s, 3 H) 2.39 (s, 3 H) 2.04 (s, 3 H); LC/MS (m/z) ES+=322 (M+1).
후처리
- temperatureThe mixture was cooled to 0° C.
- concentrationconcentrated
- dissolutionThe residue was dissolved in ethyl acetate
- washwashed with water, brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- temperaturethe mixture was heated at 120° C. for 1 hour
- stirringthe mixture was stirred at 120° C. overnight
- customreaction
- concentrationThe mixture was concentrated
- dissolutionthe residue was dissolved in ethyl acetate
- washThe organic phase was washed with water
- dry with materialbrine, dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified on silica gel (0-60% EA on hexane)
출처 및 근거
- ORD 기록
- ord-cbc2c3b3df704f6b81f3f3bcbaee0164
- 출처 데이터셋
- uspto-grants-2015_05
- 특허 번호
- US09029391B2
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