Water → HCID 20364661, 화합물

HRID 225777

반응식

HRID 225777 반응식
[C:1]1([SH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl[C:9]1[S:10][C:11]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[C:12]([CH3:14])[N:13]=1.O>CN(C)C=O>[CH3:14][C:12]1[N:13]=[C:9]([S:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[S:10][C:11]=1[C:15]([O:17][CH2:18][CH3:19])=[O:16]

참가 물질

5

반응물 3

HCID 962WaterHCID 7969ThiophenolHCID 594903Ethyl 2-chloro-4-methyl-1,3-thiazole-5-carboxylate

생성물 1

HCID 20364661HCID 20364661, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

Thiophenol (1.90 ml) was dissolved in N,N-dimethylformamide (10 ml) Sodium hydride (60% oil suspension, 740 mg) was added by portions under ice-cooling, and the mixture was stirred at room temperature for 15 min. Thereafter, a solution of ethyl 2-chloro-4-methylthiazole-5-carboxylate (3.05 g) in N,N-dimethylformamide (10 ml) was added dropwise, and the mixture was stirred at the same temperature for 20 min. Water (50 ml) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (50 ml). The ethyl acetate layer was washed twice with water (50 ml) and then with saturated brine (30 ml), and dried (Na2SO4). Ethyl acetate was evaporated under reduced pressure and the obtained residue was purified by column chromatography to give ethyl 4-methyl-2-phenylsulfanylthiazole-5-carboxylate (3.85 g).

후처리

  1. additionwas added by portions under ice-
  2. temperaturecooling
  3. stirringthe mixture was stirred at the same temperature for 20 min
  4. extractionthe mixture was extracted with ethyl acetate (50 ml)
  5. washThe ethyl acetate layer was washed twice with water (50 ml)
  6. dry with materialwith saturated brine (30 ml), and dried (Na2SO4)
  7. customEthyl acetate was evaporated under reduced pressure
  8. customthe obtained residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-d4501c3e611d4c658621a081bd183b26
출처 데이터셋
uspto-grants-2009_07
특허 번호
US07557123B2

연결된 노트

불러오는 중…