تفاعل #1851976

ord-ea2841c03dfc45ac9ae0973040dc1a65

معادلة التفاعل

O=C1CCSc2ccc(F)cc2N1
7-fluoro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
COCC[O][AlH2-][O]CCOC.[Na+]
Red-Al
[Na+].[OH-]
sodium hydroxide
Fc1ccc2c(c1)NCCCS2
7-fluoro-2,3,4,5-tetrahydro-1,5-benzothiazepine
المردود 93.0%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to room temperature
  2. 2
    درجة الحرارةThe reaction was heated
  3. 3
    درجة الحرارةat reflux for 1.5 hours
  4. 4
    استخلاصextracted with dichloromethane (3×25 mL)
  5. 5
    غسيلwashed with water
  6. 6
    تجفيفdried (sodium sulfate)
  7. 7
    أخرىThe concentrated organics were purified by preparative thin layer chromatography on silica gel
  8. 8
    غسيلeluted with 50% ethyl acetate in hexanes

الإجراء التجريبي

7-fluoro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one (76 mg, 0.38 mmol) dissolved in toluene (1 mL) and cooled to 0° C. in an ice bath. Red-Al (275 mL, 0.91mmol) was added and then the reaction allowed to warm to room temperature. The reaction was heated at reflux for 1.5 hours. 1 N sodium hydroxide was added slowly until pH>10, this was stirred for 10 minutes, extracted with dichloromethane (3×25 mL), washed with water, and dried (sodium sulfate). The concentrated organics were purified by preparative thin layer chromatography on silica gel and eluted with 50% ethyl acetate in hexanes to give 7-fluoro-2,3,4,5-tetrahydro-1,5-benzothiazepine (30.8 mg, 93%). 1H NMR (CDCl3, 300 MHz): δ 7.32 (t, 1H, J=7.5 Hz), 6.53-6.42 (m, 2H), 4.09 (s-broad, 1H), 3.31-3.27 (m, 2H), 2.83-2.79 (m, 2H), 2.11-2.04 (m, 2H) ppm.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE039680E1uspto-grants-2007_06