Piperidine → 2-Chloro-6-nitro-4-piperidinoquinazoline

To 367 mg (1.77 mmol) of 6-nitroquinazoline-2,4 (1H,3H)-dione was added 15.13 g (98.70 mmol) of phosphorus oxychloride to effect reaction in the same manner as in Example 10. Next, to the reaction mixture was added dropwise 301 mg (3.54 mmol) of piperidine under ice cooling, and the resulting mixture was stirred under ice cooling for 2 hours. Water was added to the reaction mixture, and crystals thus precipitated were filtered out to obtain 2-chloro-6-nitro-4-piperidinoquinazoline. The compound was dissolved in 1 ml of DMF, and after 1.52 g (26.65 mmol) of allylamine was added to the resulting solution, the resulting mixture was stirred at room temperature for 2.5 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 213 mg (yield: 38.4%) of the title compound.

1. customreaction in the same manner as in Example 10
2. customthus precipitated
3. filtrationwere filtered out

ORDレコード

ord-8d9ae0c038e542ffa98a4345f542b98d

出典データセット

uspto-grants-2002_01

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06339089B2