반응 #2271678

ord-2fb149862da14b85a974cc7cfdc0ad9a

반응 방정식

Fc1ccc2c(C3CCNCC3)n[nH]c2c1
6-fluoro-3-(4-piperidinyl)-1H-indazole
O=C([O-])[O-].[K+].[K+]
K2CO3
COc1cc(C(C)=O)ccc1OCCCCl
1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone
CC#N
acetonitrile
COc1cc(C(C)=O)ccc1OCCCN1CCC(c2n[nH]c3cc(F)ccc23)CC1
desired product
수율 80.8%
COc1cc(C(C)=O)ccc1OCCCN1CCC(c2n[nH]c3cc(F)ccc23)CC1
1-[4-[3-[4-(6-Fluoro-1H-indazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]-ethanone
수율 80.8%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the resulting white solid, which precipitated from solution
  2. 2
    기타was collected

실험 절차

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1H-indazole (3.5 g, 16 mmol). K2CO3 (2.2 g). 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (3.8 g, 16 mmol) and acetonitrile (90 ml) was refluxed for 16 hours. The reaction was poured into water and the resulting white solid, which precipitated from solution, was collected to afford 5.5 g of the desired product. The compound was recrystallized from dimethylformamide (twice) to afford 3.0 g (44%) of 1-[4-[3-[4-(6-fluoro-1H-indazol-3-yl)-1-piperidinyl]propoxy]-methoxyphenyl]ethanone as a white solid, m.p.=202°-204° C.

출처

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