Boron trifluoride → 1-(2-Methyloxazol-4-yl)cyclopropanamine

HRID 555173ノート

反応式

HRID 555173 の反応式
[CH3:1][C:2]1[O:3][CH:4]=[C:5]([C:7]#[N:8])[N:6]=1.[CH2:9]([Mg]Br)[CH3:10].B(F)(F)F.[OH-].[Na+]>C1COCC1.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].O>[CH3:1][C:2]1[O:3][CH:4]=[C:5]([C:7]2([NH2:8])[CH2:10][CH2:9]2)[N:6]=1

参加物

8

実験手順

2-Methyloxazole-4-carbonitrile (5 g, 46.1 mmol, 1 eq) was dissolved in dry THF at room temperature, and to which titanium(IV) isopropoxide (16 ml, 655 mmol, 1.2 eq) was added dropwise over a period of 15 minutes. The resulting mixture was stirred for 10 min and ethyl magnesium bromide (85 ml, 17 volumes) was added slowly dropwise at ambient temperature and the reaction was stirred for 1 h. Later BF3.etherate (16.7 ml, 115 mmol, 2.5 eq) was added slowly at ambient temperature and the above solution was stirred at ambient temperature for 3 h. Finally water was added and the pH was brought to 10 using 10% sodium hydroxide solution. The reaction mixture was extracted with dichloromethane, concentrated and purified by combiflash chromotography. Yield: 1.5 g (20%). 1H NMR (400 MHz, DMSO-d6): δ 0.93 (m, 2H), 1.00 (m, 2H), 1.98 (br s, 2H), 2.39 (s, 3H), 7.33 (s, 1H). LCMS: (ES+) m/z=138.9 (M+H).

後処理

  1. stirringthe reaction was stirred for 1 h
  2. additionetherate (16.7 ml, 115 mmol, 2.5 eq) was added slowly at ambient temperature
  3. stirringthe above solution was stirred at ambient temperature for 3 h
  4. extractionThe reaction mixture was extracted with dichloromethane
  5. concentrationconcentrated
  6. custompurified by combiflash chromotography

出典と根拠

ORDレコード
ord-8cde5470d73b401ba4b69213f05d5bd9
出典データセット
uspto-grants-2011_11
特許番号
US08048887B2

反応ノート

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