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5-(2-Methoxy-4-nitro-phenyl)-2,4-dimethyl-thiazole → 4-(2,4-Dimethyl-thiazol-5-yl)-3-methoxy-phenylamine

HRID 1855507
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HRID 1855507 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([N+:9]([O-])=O)[CH:6]=[CH:5][C:4]=1[C:12]1[S:16][C:15]([CH3:17])=[N:14][C:13]=1[CH3:18]>C(O)C>[CH3:17][C:15]1[S:16][C:12]([C:4]2[CH:5]=[CH:6][C:7]([NH2:9])=[CH:8][C:3]=2[O:2][CH3:1])=[C:13]([CH3:18])[N:14]=1
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참가 물질

3

반응물 1

HCID 670961295-(2-Methoxy-4-nitro-phenyl)-2,4-dimethyl-thiazole

생성물 1

HCID 670962794-(2,4-Dimethyl-thiazol-5-yl)-3-methoxy-phenylamine수율 75%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 5-(2-methoxy-4-nitro-phenyl)-2,4-dimethyl-thiazole (415 mg, 1.57 mmol) and anhydrous stannous chloride (1.52 g, 7.85 mmol) in ethanol (25 mL) was stirred at reflux for 3 hours. The yellow solution was evaporated and the residue dissolved in ethyl acetate. This solution was washed with 1N aqueous sodium hydroxide solution, twice with water, with brine, dried with magnesium sulfate and the solvent was evaporated to dryness. Column chromatography (50 g silica, heptane/ethyl acetate 30-60% v/v) afforded the title compound (276 mg, 75%) as a pale yellow solid. MS ISP (m/e): 235.2 [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.04 (d, 1H), 6.31 (m, 2H), 3.80 (s broad, 2H), 3.78 (s, 3H), 2.66 (s, 3H), 2.29 (s, 3H). Mp 112-115° C.

후처리

  1. temperatureat reflux for 3 hours
  2. customThe yellow solution was evaporated
  3. dissolutionthe residue dissolved in ethyl acetate
  4. washThis solution was washed with 1N aqueous sodium hydroxide solution, twice with water, with brine
  5. dry with materialdried with magnesium sulfate
  6. customthe solvent was evaporated to dryness

출처 및 근거

ORD 기록
ord-4d50734d32bc4adf810f27739d6bd6d3
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962834B2

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