Reacción #437960

ord-e4d211b2ad77433f9fc47917c774b142

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISTILLATIONof freshly distilled) and
  2. 2
    OtroThe flask was removed from the ice bath
  3. 3
    Temperaturato warm to room temperature
  4. 4
    workup.ADDITIONWater (0.08 mL) was added
  5. 5
    workup.STIRRINGstirred for 10 minutes
  6. 6
    workup.ADDITION15% sodium hydroxide (0.08 mL) was added
  7. 7
    workup.STIRRINGstirred for 10 minutes
  8. 8
    workup.ADDITIONWater (0.024 mL) was added
  9. 9
    workup.STIRRINGstirred for 10 minutes
  10. 10
    ExtracciónThe reaction was extracted with dichloromethane (2×25 mL)
  11. 11
    ConcentraciónThe organics were concentrated to a residue
  12. 12
    workup.ADDITIONhydrogen chloride in ether (1 M) was added until precipatation
  13. 13
    Otroformed
  14. 14
    Filtraciónthe precipatate was filtered off

Procedimiento

7-fluoro-5-nitroso-2,3,4,5-tetrahydro-1,5-benzothiazepine (449 mg, 2.11 mmol) was suspended in THF (1 mL of freshly distilled) and cooled to 0° C. in an ice bath. Lithium aluminum hydride (80 mg, 2.11 mmol) was added in a portion-wise fashion. The flask was removed from the ice bath and allowed to warm to room temperature and was stirred for 2 hours. Water (0.08 mL) was added and stirred for 10 minutes. 15% sodium hydroxide (0.08 mL) was added stirred for 10 minutes. Water (0.024 mL) was added and stirred for 10 minutes. The reaction was extracted with dichloromethane (2×25 mL). The organics were concentrated to a residue, then taken up in minimal amount of dichloromethane and then hydrogen chloride in ether (1 M) was added until precipatation formed, the precipatate was filtered off to give 7-fluoro-3,4-dihydro-1,5-benzothiazepin-5(2H)-amine (471 mg, 95%). 1H NMR (CD-3OD, 300 MHz): δ 7.59 (t, 1H, J=7.5 Hz), 7.28 (d, 1H, J=9.9 Hz), 7.00 (t, 1H, J=8.2 Hz), 3.52 (t, 1H, J=7.5 Hz), 2.92–2.86 (m, 1H), 2.72–2.70 (m, 2H), 2.40–2.31 (m, 1H), 2.2–2.18 (m, 2H) ppm.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07183282B2uspto-grants-2007_02