3-Aminopyridine → 6-(2,6-Dichlorophenyl)-8-methyl-2-(pyridin-3-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

HRID 1586426

反応式

HRID 1586426 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14](SC)[N:15]=[CH:16][C:11]=2[CH:10]=1.[NH2:23][C:24]1[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=1.Cl.NC1C=NC=CC=1>O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14]([NH:23][C:24]3[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=3)[N:15]=[CH:16][C:11]=2[CH:10]=1

参加物

5

反応条件

温度
210 °C

実験手順

A mixture of 0.165 g (0.47 mmol) of 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one, 0.500 g (5.30 mmol) of 3-aminopyridine base, and 0.066 g (0.50 mmol) of 3-aminopyridine hydrochloride was heated with stirring in a 210° C. oil bath for 1 hour. Water (5 mL) was added to the cooled reaction mixture to precipitate a solid. The solid was filtered, washed well with water, and dried; wt 0.147 g. Purification was effected by silica gel chromatography by eluting with chloroform and then ethyl acetate. The ethyl acetate eluent containing the pure product was concentrated to 2 mL volume. The crystals that separated on inducement were filtered and washed with 0.5 mL of ethyl acetate and 1 mL of ether; wt 0.810 g; mp 247-248° C.

後処理

  1. temperaturewas heated
  2. customto precipitate a solid
  3. filtrationThe solid was filtered
  4. washwashed well with water
  5. customdried
  6. customPurification
  7. washby eluting with chloroform
  8. additionThe ethyl acetate eluent containing the pure product
  9. concentrationwas concentrated to 2 mL volume
  10. customThe crystals that separated on inducement
  11. filtrationwere filtered
  12. washwashed with 0.5 mL of ethyl acetate and 1 mL of ether

出典と根拠

ORDレコード
ord-a63304464a4f4ff992dadde212713ec6
出典データセット
uspto-grants-1999_08
特許番号
US05945422

関連ノート

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