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Trifluoroacetic acid → N-(2,4-dichloro-thiazol-5-yl)-3-methylsulfanyl-propionamide

HRID 533337
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HRID 533337 반응식
C(OC(=O)[N:7]([C:14]1[S:18][C:17]([Cl:19])=[N:16][C:15]=1[Cl:20])[C:8](=[O:13])[CH2:9][CH2:10][S:11][CH3:12])(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[Cl:19][C:17]1[S:18][C:14]([NH:7][C:8](=[O:13])[CH2:9][CH2:10][S:11][CH3:12])=[C:15]([Cl:20])[N:16]=1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 59580673HCID 59580673, 화합물

생성물 1

HCID 59580948N-(2,4-dichloro-thiazol-5-yl)-3-methylsulfanyl-propionamide수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (2,4-dichloro-thiazol-5-yl)-(3-methylsulfanyl-propionyl)-carbamic acid tert-butyl ester (1.10 g, 2.97 mmol) in DCM (10 mL) was added trifluoroacetic acid (3.4 g, 2,2 mL, 30 mmol). The solution was stirred at room temperature for 15 minutes, before it was quenched slowly with saturated NaHCO3 solution. The organic layer was separated and the aqueous layer was extracted with 20 mL DCM. The combined organic layer was dried over Na2SO4 and purified by silica gel chromatography (0 to 100% ethyl acetate/hexanes) to give product as a white solid (612 mg, 76%): 1H NMR (300 MHz, CDCl3) δ 8.79 (s, 1H), 2.90 (t, J=7.2 Hz, 2H), 2.79 (t, J=7.2 Hz, 2H), 2.29 (s, 3H); ESIMS m/z 271.0 (M+1).

후처리

  1. customwas quenched slowly with saturated NaHCO3 solution
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with 20 mL DCM
  4. dry with materialThe combined organic layer was dried over Na2SO4
  5. custompurified by silica gel chromatography (0 to 100% ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-b3c452d17d204cad83d5006f1d1856af
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853246B2

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