تفاعل #2028939

ord-49342d5482bb4e368c32efa1a2bf9d64

معادلة التفاعل

Cl.c1ccc2c(c1)N=C(N1CCNCC1)c1ccccc1S2
11-piperazin-1-yldibenzo[b,f][1,4]thiazepine hydrochloride
c1ccc2c(c1)N=C(N1CCNCC1)c1ccccc1S2
11-piperazin-1-yldibenzo[b,f][1,4]thiazepine

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىevaporated to dryness on a rotary evaporator
  2. 2
    workup.ADDITIONThe resulting hard solid was then charged to a jacketed vessel
  3. 3
    درجة الحرارةcooled to 5° C.
  4. 4
    workup.WAITheld for 4 h

الإجراء التجريبي

The above procedure was repeated for an additional four aqueous solutions of 11-piperazin-1-yldibenzo[b,f][1,4]thiazepine hydrochloride and the five resulting toluene solutions were combined and evaporated to dryness on a rotary evaporator. The resulting hard solid was then charged to a jacketed vessel and slurried with methyl-t-butyl ether (MTBE) (500 mL). The resulting slurry was stirred overnight at ambient temperature and then cooled to 5° C. and held for 4 h. The solid 11-piperazin-1-yldibenzo[b,f][1,4]thiazepine product was isolated on a no. 3 sinter and washed with 200 mL of cold MTBE. The cake was dried in a vacuum oven overnight at 60° C. yielding 373 g of product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08389510B2uspto-grants-2013_03