2,5-Dihydrofuran → N-(4-(3-(2,3-Dihydrofuran-2-YL)pyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amine

HRID 410291

反応式

HRID 410291 の反応式
I[C:2]1[C:3]([O:8][C:9]2[CH:14]=[CH:13][C:12]([NH:15][C:16]3[S:17][C:18]4[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=4[N:20]=3)=[CH:11][CH:10]=2)=[N:4][CH:5]=[CH:6][CH:7]=1.CN(C1CCCCC1)C1CCCCC1.[O:39]1[CH2:43][CH:42]=[CH:41][CH2:40]1>O1CCOCC1.CO.CC(C)([P](C(C)(C)C)([Pd][P](C(C)(C)C)(C(C)(C)C)C(C)(C)C)C(C)(C)C)C>[O:39]1[CH:40]=[CH:41][CH2:42][CH:43]1[C:2]1[C:3]([O:8][C:9]2[CH:14]=[CH:13][C:12]([NH:15][C:16]3[S:17][C:18]4[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=4[N:20]=3)=[CH:11][CH:10]=2)=[N:4][CH:5]=[CH:6][CH:7]=1

参加物

7

実験手順

A mixture of N-(4-(3-iodopyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine (0.403 g, 0.905 mmol), N-methyldicyclohexylamine (0.400 mL, 1.886 mmol, Aldrich), bis(tri-tert-butylphosphine)palladium (0) (0.045 g, 0.088 mmol, Strem) and 2,5-dihydrofuran (0.500 mL, 6.78 mmol, Aldrich) in 5 mL of dioxane was capped under an atmosphere of argon and stirred at rt for 3 h and then heated at 45° C. overnight. The reaction mixture was diluted with MeOH, evaporated onto silica gel and purified by flash chromatography (Isco, (40 gram)) eluting with 2M NH3 in MeOH:CH2Cl2 (0:1→3:97) to give a white amorphous solid. MS (ESI, pos. ion) m/z: 386.0 (M+1).

後処理

  1. customwas capped under an atmosphere of argon
  2. temperatureheated at 45° C. overnight
  3. customevaporated onto silica gel
  4. custompurified by flash chromatography (Isco, (40 gram))
  5. washeluting with 2M NH3 in MeOH:CH2Cl2 (0:1→3:97)
  6. customto give a white amorphous solid

出典と根拠

ORDレコード
ord-f0fe03bd2a96425aac84f25f34cc687c
出典データセット
uspto-grants-2014_06
特許番号
US08759532B2

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