반응 #495737

ord-b80338c9e80140eba55575f268e977e7

반응 방정식

Cl
hydrochloric acid
Cc1n[nH]c2ccc(C=O)cc12
3-methyl-1H-indazole-5-carbaldehyde
O=C1COC(=O)C1
furan-2,4(3H,5H)-dione
N#CC=C(N)C(F)(F)F
3-amino-4,4,4-trifluorobut-2-enenitrile
Cc1n[nH]c2ccc(C3C(C#N)=C(C(F)(F)F)NC4=C3C(=O)OC4)cc12
title compound
Cc1n[nH]c2ccc(C3C(C#N)=C(C(F)(F)F)NC4=C3C(=O)OC4)cc12
4-(3-Methyl-1H-indazol-5-yl)-5-oxo-2-(trifluoromethyl)-1,4,5,7-tetrahydrofuro[3,4-b]pyridine-3-carbonitrile

반응 조건

온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe mixture was stirred at 100° C. for another 1 h
  2. 2
    온도After cooling
  3. 3
    기타the mixture was directly purified by RP-HPLC (acetonitrile/water+0.1% TFA gradient)

실험 절차

100 mg (0.624 mmol) 3-methyl-1H-indazole-5-carbaldehyde (Example 1A) and 62.5 mg (0.624 mmol) furan-2,4(3H,5H)-dione were heated up to reflux in 1-pentanol (3 ml) for 1 h. After addition of 425 mg (3.120 mmol) 3-amino-4,4,4-trifluorobut-2-enenitrile [A. W. Lutz, U.S. Pat. No. 3,635,977], the reaction mixture was stirred at 100° C. for further 4 h. Then, conc. hydrochloric acid (115 μl) and water (350 μl) were added, and the mixture was stirred at 100° C. for another 1 h. After cooling, the mixture was directly purified by RP-HPLC (acetonitrile/water+0.1% TFA gradient) to give 33 mg (14% of th.) of the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08759341B2uspto-grants-2014_06