Phenyl isocyanate → 7a-(3-propyl-5-isoxazolyl)-hexahydro-1H-pyrrolizine

HRID 3303

反応式

HRID 3303 の反応式
[N+:1]([CH2:4][CH2:5][CH2:6][CH3:7])([O-])=[O:2].C1(N=C=O)C=CC=CC=1.[C:17]([C:19]12[CH2:26][CH2:25][CH2:24][N:23]1[CH2:22][CH2:21][CH2:20]2)#[CH:18]>C1C=CC=CC=1>[CH2:5]([C:4]1[CH:18]=[C:17]([C:19]23[CH2:26][CH2:25][CH2:24][N:23]2[CH2:22][CH2:21][CH2:20]3)[O:2][N:1]=1)[CH2:6][CH3:7]

参加物

5

反応物 3

HCID 7672Phenyl isocyanateHCID 123021-NitrobutaneHCID 195976957a-ethynylhexahydro-1H-pyrrolizine

生成物 1

HCID 189347247a-(3-propyl-5-isoxazolyl)-hexahydro-1H-pyrrolizine収率 53.4%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

Nitrobutane (0.705 mL, 6.66 mmol) and phenylisocyanate (1.50 mL, 13.3 mmol) were dissolved in benzene (13.5 mL) and added to a flask containing 7a-ethynyl-hexahydro-1H-pyrrolizine (450 mg, 3.33 mmol, from step 13a). The solution was stirred at ambient temperature for 1 hour and at reflux for 5 hours. The mixture was cooled, filtered, concentrated and diluted with EtOAc. The solution was extracted with 6N HCl. The aqueous phase was made basic with 15% NaOH and extracted with methylene chloride. The organic extracts were combined, dried (MgSO4) and concentrated. The residue was residue was chromatographed (silica gel; CHCl3 /MeOH, 98:2) to afford an amber oil (392 mg, 53%). 1H NMR (CDCl3, 300 MHz) δ0.97 (t, J=7.5 Hz, 3H), 1.61-1.92 (m, 8H), 2.15-2.26 (m, 2H), 2.55-2.69 (m, 4H), 3.13-3.20 (m, 2H), 5.96 (s, 1H); MS (CI/NH3) m/z: 221 (M+H)+.

後処理

  1. additionadded to a flask
  2. temperatureat reflux for 5 hours
  3. temperatureThe mixture was cooled
  4. filtrationfiltered
  5. concentrationconcentrated
  6. additiondiluted with EtOAc
  7. extractionThe solution was extracted with 6N HCl
  8. extractionextracted with methylene chloride
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated
  11. customwas chromatographed (silica gel; CHCl3 /MeOH, 98:2)

出典と根拠

ORDレコード
ord-bbc0aabc6c144848bb5aa35cb5124c07
出典データセット
uspto-grants-1998_03
特許番号
US05733912

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