반응 #2271671

ord-2eaac86dc63841d1bbf7b1a8c1c0f630

반응 방정식

Fc1ccc2onc(C3CCNCC3)c2c1
5-fluoro -3-(4-piperidinyl)-1,2-benzisoxazole
COc1cc(C(C)=O)ccc1OCCCCl
1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone
O=C([O-])[O-].[K+].[K+]
K2CO3
CC#N
acetonitrile
COc1cc(C(C)=O)ccc1OCCCN1CCC(c2noc3ccc(F)cc23)CC1
white solid
수율 93.8%
COc1cc(C(C)=O)ccc1OCCCN1CCC(c2noc3ccc(F)cc23)CC1
1-[4-[3-[4-(5-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxy-phenyl]ethanone
수율 93.8%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도refluxed for 8 hours
  2. 2
    추출the aqueous mixture was extracted with ethyl acetate
  3. 3
    추출The ethyl acetate extract
  4. 4
    세척was washed (brine)
  5. 5
    건조dried (MgSO4)
  6. 6
    농축concentrated

실험 절차

A mixture of 5-fluoro -3-(4-piperidinyl)-1,2-benzisoxazole (2.2 g, 10 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (2.4 g, 10 mmol). K2CO3 (1.4 g), a few crystals of Kl and acetonitrile (100 ml) was stirred and refluxed for 8 hours. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate extract was washed (brine), dried (MgSO4), and concentrated to afford 4.0 g of a white solid. The solid was chromatographed on a Waters Prep 500 HPLC utilizing silica get columns and eluting with methylene chloride/methanol (5%). Concentration of the appropriate fractions afforded 2.0 g (47%) of 1-[4-[3-[4-(5-fluoro-1,2-benzisoxazol-3-yl)-1-methoxyphenyl]ethanone as a white crystalline solid, m.p.=103°-105° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE037729E1uspto-grants-2002_06