반응 #46695

ord-d0c278f7542944b1998097f49931c896

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled
  2. 2
    기타The cooling bath was removed
  3. 3
    workup.STIRRINGthe mixture stirred at room temperature for 1 h
  4. 4
    workup.ADDITIONThe reaction mixture was diluted with dichloromethane (50 ml)
  5. 5
    세척washed with 1 M hydrochloric acid (2×50 ml)
  6. 6
    기타The organic layer was separated
  7. 7
    건조dried over sodium sulphate
  8. 8
    기타evaporated under reduced pressure

실험 절차

2-Aminoindan hydrochloride (5.16 g, 30 mmol, Sigma Aldrich Company Ltd.) was suspended in dry dichloromethane (100 ml), and cooled with stirring under argon to 0° C. To the suspension was added 1,8-diazabicyclo[5.4.0]undec-7-ene (14 g, 92 mmol) followed by the dropwise addition of isopropylsulfonyl chloride (8.56 g, 60 mmol). The cooling bath was removed and the mixture stirred at room temperature for 1 h. The reaction mixture was diluted with dichloromethane (50 ml) and washed with 1 M hydrochloric acid (2×50 ml). The organic layer was separated, dried over sodium sulphate and evaporated under reduced pressure to give a yellow oil (11.8 g). The crude product was purified by chromatography on a 50 g Isolute™ Flash silica-gel column eluting from 20-50% ethyl acetate in 40-60° C. petroleum ether to give the title compound as a pale yellow solid (6.88 g, 96%); 1H-NMR (400 MHz, CDCl3) δ 1.39 (6H, d, J=7 Hz), 2.91 (2H, m), 3.18 (1H, m), 3.31 (2H, m), 4.31 (2H, m), 7.21 (4H, m).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741351B2uspto-grants-2010_06