تفاعل #2186191

ord-18eefd571c03425384bca27ebde444a8

معادلة التفاعل

O=Cc1ccc(N2CCN(CCF)CC2)cc1O
4-[4-(2-Fluoro-ethyl)-piperazin-1-yl]-2-hydroxy-benzaldehyde
COC(=O)Cc1nc2ccccc2s1
benzothiazol-2-yl-acetic acid methyl ester
C1CCNCC1
piperidine
O=c1oc2cc(N3CCN(CCF)CC3)ccc2cc1-c1nc2ccccc2s1
desired product
المردود 55.0%
O=c1oc2cc(N3CCN(CCF)CC3)ccc2cc1-c1nc2ccccc2s1
3-Benzothiazol-2-yl-7-[4-(2-fluoro-ethyl)-piperazin-1-yl]-chromen-2-one
المردود 55.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto reach room temperature
  2. 2
    ترشيحthe precipitate filtered off
  3. 3
    غسيلwashed with diethylether
  4. 4
    أخرىdried under high vacuum

الإجراء التجريبي

200 mg (0.793 mmol) 4-[4-(2-Fluoro-ethyl)-piperazin-1-yl]-2-hydroxy-benzaldehyde and 164 mg (1 eq.) benzothiazol-2-yl-acetic acid methyl ester are heated to reflux for 3 h in 5 mL benzene and 2.5 mL acetonitrile, in the presence of 0.157 mL (2 eq.) piperidine. The reaction mixture is allowed to reach room temperature and the precipitate filtered off, washed with diethylether and dried under high vacuum to yield 90 mg (55%) of desired product as a yellow powder (melting point: 246° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07569337B2uspto-grants-2009_08