methyl-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-amine → 2,N-dimethyl-N-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-3-methylsulfanyl-propionamide

HRID 1428329노트

반응식

HRID 1428329 반응식
[CH3:1][NH:2][C:3]1[N:4]([CH3:14])[N:5]=[C:6]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)[CH:7]=1.[CH3:15][CH:16]([CH2:20][S:21][CH3:22])[C:17](Cl)=[O:18]>ClC(Cl)C>[CH3:15][CH:16]([CH2:20][S:21][CH3:22])[C:17]([N:2]([CH3:1])[C:3]1[N:4]([CH3:14])[N:5]=[C:6]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)[CH:7]=1)=[O:18]

참가 물질

4

반응물 2

HCID 67499915methyl-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-amineHCID 758176512-Methyl-3-(methylthio)propanoyl chloride

생성물 1

HCID 674994562,N-dimethyl-N-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-3-methylsulfanyl-propionamide

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매2회

실험 절차

To a solution of methyl-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-amine (150 mg, 0.8 mmol) under N2 in ice-cold dichloroethane (DCE; 2 mL) was added dropwise via pipette a solution of 2-methyl-3-methylsulfanyl-propionylchloride (146 mg, 0.9 mmol) in DCE (1.5 mL). After stirring for 10 minutes (min), a solution of 4-N,N-dimethylaminopyridine (DMAP; 107 mg, 0.9 mmol) in DCE (2 mL) was added dropwise. The ice bath was removed after 30 min, and the mixture was stirred at room temperature for 90 min and then at reflux for 14 h. The mixture was concentrated under reduced pressure and was purified by silica gel chromatography eluting with a gradient of EtOAc in hexane. The product, 2,N-dimethyl-N-(2-methyl-5-pyridin-3-yl-2H-pyrazol-3-yl)-3-methylsulfanyl-propionamide, was isolated as a yellow semi-solid (44 mg, 24%): 1H NMR (400 MHz, CDCl3) δ 9.00 (s, 1H), 8.58 (s, 1H), 8.08 (br d, J=7.0 Hz, 1H), 7.35 (br dd, J=7.3, 4.8 Hz, 1H), 6.58 (br s, 0.5H), 6.49 (br s, 0.5H), 3.89-3.79 (m, 3H), 3.25 (s, 3H), 2.96-2.80 (m, 1H), 2.42-2.40 (m, 1H), 2.02-1.99 (m, 3H), 2.62 (m, 1H), 1.15 (d, J=6.0 Hz, 3H); MS (m/z) 305.0 [M+1].

후처리

  1. customThe ice bath was removed after 30 min
  2. stirringthe mixture was stirred at room temperature for 90 min
  3. temperatureat reflux for 14 h
  4. concentrationThe mixture was concentrated under reduced pressure
  5. customwas purified by silica gel chromatography
  6. washeluting with a gradient of EtOAc in hexane

출처 및 근거

ORD 기록
ord-b48f40cb809e4c0685d6242634018afd
출처 데이터셋
uspto-grants-2015_01
특허 번호
US08937083B2

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