تفاعل #42665

ord-844c3cb212af48758b40eb851b8c0f3f

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزthe mixture was concentrated at 25° C.
  2. 2
    workup.ADDITIONmethanol (150 mL) was added
  3. 3
    ترشيحthe precipitate filtered
  4. 4
    تركيزThe filtrate was concentrated
  5. 5
    workup.ADDITIONdiluted with dichloromethane (100 mL)
  6. 6
    غسيلwashed with water (2×), saturated aqueous sodium bicarbonate (2×), saturated brine
  7. 7
    تجفيفdried over magnesium sulfate
  8. 8
    ترشيحfiltered
  9. 9
    تركيزconcentrated
  10. 10
    أخرىPurification by silica gel chromatography (5% ethyl acetate/hexanes→65% ethyl acetate/hexanes)

الإجراء التجريبي

Trifluoroacetic acid (60 mL) was added to a solution of benzyl (3R)-6-(2,3-difluorophenyl)-1-(2,4-dimethoxybenzyl)-2-oxo-2,3,4,7-tetrahydro-1H-azepin-3-ylcarbamate (3.70 g, 7.08 mmol) in dichloromethane (40 mL). After 18 h, the mixture was concentrated at 25° C., methanol (150 mL) was added, and the precipitate filtered. The filtrate was concentrated, diluted with dichloromethane (100 mL), washed with water (2×), saturated aqueous sodium bicarbonate (2×), saturated brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (5% ethyl acetate/hexanes→65% ethyl acetate/hexanes) gave the title compound (1.75 g). MS 373.1 (M+1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07732438B2uspto-grants-2010_06