Reacción #437960
ord-e4d211b2ad77433f9fc47917c774b142
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.DISTILLATIONof freshly distilled) and
- 2OtroThe flask was removed from the ice bath
- 3Temperaturato warm to room temperature
- 4workup.ADDITIONWater (0.08 mL) was added
- 5workup.STIRRINGstirred for 10 minutes
- 6workup.ADDITION15% sodium hydroxide (0.08 mL) was added
- 7workup.STIRRINGstirred for 10 minutes
- 8workup.ADDITIONWater (0.024 mL) was added
- 9workup.STIRRINGstirred for 10 minutes
- 10ExtracciónThe reaction was extracted with dichloromethane (2×25 mL)
- 11ConcentraciónThe organics were concentrated to a residue
- 12workup.ADDITIONhydrogen chloride in ether (1 M) was added until precipatation
- 13Otroformed
- 14Filtraciónthe 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.