反応 #2298662

ord-6ca490f2e3be407b907e3f6d8e9c20cf

反応方程式

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
収率 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
収率 80.8%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was refluxed for 16 hours
  2. 2
    その他the resulting white solid, which precipitated from solution
  3. 3
    その他was collected

実験手順

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1H-indazole (3.5 g, 0.016 mol), K2CO3 (2.2 g), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (3.8 g, 0.016 mol) 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]-3-methoxyphenyl]ethanone as a white solid, m.p.=202°-204° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE039265E1uspto-grants-2006_09