Ammonium Chloride → 8-Fluoro-10,11-dihydro-5-methylene-5H-benzo[4,5]cyclohepta[1,2-b]pyridine

HRID 2218757ノート

反応式

HRID 2218757 の反応式
[F:1][C:2]1[CH:17]=[CH:16][C:5]2[C:6](=O)[C:7]3[C:8]([CH2:13][CH2:14][C:4]=2[CH:3]=1)=[N:9][CH:10]=[CH:11][CH:12]=3.[CH3:18][Mg]Br.[Cl-].[NH4+]>O1CCCC1>[F:1][C:2]1[CH:17]=[CH:16][C:5]2[C:6](=[CH2:18])[C:7]3[C:8]([CH2:13][CH2:14][C:4]=2[CH:3]=1)=[N:9][CH:10]=[CH:11][CH:12]=3

参加物

5

反応物 3

HCID 25517Ammonium ChlorideHCID 442032048-Fluoro-10,11-dihydro-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-oneHCID 178418573HCID 178418573、化合物

生成物 1

HCID 597699728-Fluoro-10,11-dihydro-5-methylene-5H-benzo[4,5]cyclohepta[1,2-b]pyridine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Chill a mixture of 8-fluoro-10,11-dihydro-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (1.3 g, 5.7 mmol) and dry tetrahydrofuran (50 mL) to 0° C. Treat this mixture with methyl magnesium bromide(3.0M solution in diethyl ether, 5.7 mL, 17.2 mmol). Remove cooling and stir the admixture at room temperature for 15 min. Quench the reaction, while cooling with an ice-water bath, by adding saturated aqueous ammonium chloride solution (50 mL). Separate the layers and extract the aqueous layer with methylene chloride (2×50 mL). Dry the combined organic layers with magnesium sulfate, filter and concentrate to provide the intermediate product as a thick crude oil.

後処理

  1. temperatureChill
  2. customRemove
  3. temperaturecooling
  4. customQuench
  5. customthe reaction
  6. temperaturewhile cooling with an ice-water bath
  7. customSeparate the layers
  8. extractionextract the aqueous layer with methylene chloride (2×50 mL)
  9. dry with materialDry the combined organic layers with magnesium sulfate
  10. filtrationfilter
  11. concentrationconcentrate
  12. customto provide the intermediate product as a thick crude oil

出典と根拠

ORDレコード
ord-003e0785793545458001c6d31ffc2406
出典データセット
uspto-grants-2008_08
特許番号
US07411072B2

反応ノート

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