Phosphorus oxychloride → HCID 59811133、化合物

反応式

[CH3:1][O:2][C:3]([C:5]1[C:6]([CH2:26][O:27][CH3:28])=[N:7][C:8]2[C:13]([C:14]=1O)=[CH:12][CH:11]=[C:10]([C:16]1[C:21]([C:22]([F:25])([F:24])[F:23])=[CH:20][CH:19]=[CH:18][N:17]=1)[N:9]=2)=[O:4].O=P(Cl)(Cl)[Cl:31]>N1C(C)=CC=CC=1C.C(Cl)(Cl)Cl>[Cl:31][C:14]1[C:13]2[C:8](=[N:9][C:10]([C:16]3[C:21]([C:22]([F:25])([F:24])[F:23])=[CH:20][CH:19]=[CH:18][N:17]=3)=[CH:11][CH:12]=2)[N:7]=[C:6]([CH2:26][O:27][CH3:28])[C:5]=1[C:3]([O:2][CH3:1])=[O:4]

参加物

実験手順

Dissolve 4-hydroxy-2-methoxymethyl-7-(3-trifluoromethylpyridin-2-yl)-[1,8]naphthyridine-3-carboxylic acid methyl ester (500 mg, 1.27 mmol) in a solution of POCl3 (0.4 mL), 2,6-lutidine (0.43 mL) and CHCl3 (25 mL). Heat the mixture at reflux overnight. Remove the solvent under reduced pressure. Partition the residue between CH2Cl2 and saturated NaHCO3 (aq). Extract the aqueous layer twice with CH2Cl2 (2×100 mL). Dry the combined organic extracts over Na2SO4. Remove the solvent under reduced pressure. Purify the crude product by preparatory TLC eluting with EtOAc\Hexanes (1:1) to yield the title compound.