Pyridine → N-methyl-2-(pyridin-3-yl)thiazol-5-amine

HRID 1803413ノート

反応式

HRID 1803413 の反応式
P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:2].[CH3:15][NH:16][C:17]([CH2:19][NH:20][C:21](=O)[C:22]1[CH:27]=[CH:26][CH:25]=[N:24][CH:23]=1)=O.N1C=CC=CC=1>C1(C)C=CC=CC=1>[CH3:15][NH:16][C:17]1[S:2][C:21]([C:22]2[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=2)=[N:20][CH:19]=1

参加物

5

実験手順

A suspension of phosphorus pentasulfide (1.73 g, 7.8 mmol) and N-methylcarbamoylmethyl-nicotinamide (1 g, 5 mmol) in dry toluene (10 mL) was stirred at reflux under nitrogen for 16 h. The mixture was cooled to room temperature and then dry pyridine (4 mL) was added. The mixture was stirred at reflux under nitrogen for 8 h, then it was cooled to room temperature and the organic layer was removed. The dark residue was treated with hot saturated aqueous sodium bicarbonate (Na2CO3, 40 mL) and the aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (50 mL), dried over magnesium sulfate (MgSO4), and purified by silica gel chromatography (1% methanol in dichloromethane) to yield a brown amorphous solid (0.22 g, 22%): mp 141-146° C.; 1H NMR (300 MHz, CDCl3) δ 8.97 (d, J=2.4 Hz, 1H), 8.53 (dd, J=5.0, 1.8 Hz, 1H), 8.06 (ddd, J=7.2, 3.3, 0.6 Hz, 1H), 7.31 (ddd, J=5.5, 4.7, 0.5 Hz, 1H), 6.96 (s, 1H), 2.97 (d, J=5.0 Hz, 3H); ESIMS m/z 192 (M+1).

後処理

  1. temperatureat reflux under nitrogen for 16 h
  2. stirringThe mixture was stirred
  3. temperatureat reflux under nitrogen for 8 h
  4. temperatureit was cooled to room temperature
  5. customthe organic layer was removed
  6. additionThe dark residue was treated with hot saturated aqueous sodium bicarbonate (Na2CO3, 40 mL)
  7. extractionthe aqueous layer was extracted with ethyl acetate (2×50 mL)
  8. washThe combined organic extracts were washed with brine (50 mL)
  9. dry with materialdried over magnesium sulfate (MgSO4)
  10. custompurified by silica gel chromatography (1% methanol in dichloromethane)

出典と根拠

ORDレコード
ord-6624554c87a449c5b64305b3af5414a8
出典データセット
uspto-grants-2013_01
特許番号
US08350044B2

反応ノート

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