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1,4-Dioxane → 3-Amino-5-bromo-1-methyl-1,2-dihydropyridin-2-one

HRID 593148
ノート
印刷プレビュー

反応式

HRID 593148 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([N:10]=C(C2C=CC=CC=2)C2C=CC=CC=2)[C:5](=[O:9])[N:6]([CH3:8])[CH:7]=1.O1CCOCC1>C(OCC)(=O)C>[NH2:10][C:4]1[C:5](=[O:9])[N:6]([CH3:8])[CH:7]=[C:2]([Br:1])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 312751,4-DioxaneHCID 866845845-bromo-3-(diphenylmethyleneamino)-1-methylpyridin-2(1H)-one

生成物 1

HCID 529112683-Amino-5-bromo-1-methyl-1,2-dihydropyridin-2-one収率 52.1%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 5-bromo-3-(diphenylmethyleneamino)-1-methylpyridin-2(1H)-one (3.82 g, 10.4 mmol) in ethyl acetate (10 mL) was added 4 MHCl/dioxane (7.8 mL, 31.3 mmol). The reaction mixture was stirred for 0.5 h and concentrated under reduced pressure. The residue was washed with tert-butyl methyl ether and filtered. The solid was dissolved in ethyl acetate (10 mL) and water (10 mL). The pH of the resulting mixture was adjusted to between 7 and 8 by adding K2CO3 gradually. The water phase was separated and extracted with dichloromethane for three times. The combined organic layer was concentrated under reduced pressure to afford 325a as a yellow solid (1.1 g, 52%). MS-ESI: [M+H]+ 202.9.

後処理

  1. concentrationconcentrated under reduced pressure
  2. washThe residue was washed with tert-butyl methyl ether
  3. filtrationfiltered
  4. dissolutionThe solid was dissolved in ethyl acetate (10 mL)
  5. additionby adding K2CO3 gradually
  6. customThe water phase was separated
  7. extractionextracted with dichloromethane for three times
  8. concentrationThe combined organic layer was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-9ff511ce15504abbb20a28f791ce8a61
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09238655B2

反応ノート

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