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Pyridine → (E)-Ethyl 3-[6-[[3,5-bis(trimethylsilyl)benzoyl]amino]pyridin-3-yl]acrylate

HRID 2265083
ノート
印刷プレビュー

反応式

HRID 2265083 の反応式
[CH3:1][Si:2]([CH3:17])([CH3:16])[C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([Si:12]([CH3:15])([CH3:14])[CH3:13])[CH:11]=1)[C:6]([OH:8])=O.N1C=CC=CC=1.[NH2:24][C:25]1[N:30]=[CH:29][C:28]([CH:31]=[CH:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])=[CH:27][CH:26]=1.P(Cl)(Cl)(Cl)=O>C(#N)C.C(OCC)(=O)C.O>[CH3:16][Si:2]([CH3:1])([CH3:17])[C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([Si:12]([CH3:15])([CH3:14])[CH3:13])[CH:11]=1)[C:6]([NH:24][C:25]1[N:30]=[CH:29][C:28](/[CH:31]=[CH:32]/[C:33]([O:35][CH2:36][CH3:37])=[O:34])=[CH:27][CH:26]=1)=[O:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 1049PyridineHCID 24813Phosphorus oxychlorideHCID 146056473,5-Bis(trimethylsilyl)benzoic acid2 回HCID 53409341Ethyl 3-(6-aminopyridine-3-yl)acrylate

生成物 1

HCID 86644273(E)-Ethyl 3-[6-[[3,5-bis(trimethylsilyl)benzoyl]amino]pyridin-3-yl]acrylate収率 20%

試薬・触媒・溶媒 3

HCID 962
Water
溶媒
HCID 6342Acetonitrile溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

3,5-Bis(trimethylsilyl)benzoic acid (hereinafter referred to as “BTMB”; 700 mg) was suspended in acetonitrile (5.25 ml) in a nitrogen atmosphere. Pyridine (0.212 ml) and Compound 1a (603 mg) were added to the suspension, and phosphorus oxychloride (0.131 ml) was added dropwise under ice-cooling. The mixture was stirred while refluxing under heating for 3.5 hours. After the reaction mixture was allowed to cool, water and ethyl acetate were added thereto. The organic layer was washed three times with water and once with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by neutral silica gel column chromatography (5% ethyl acetate/n-hexane) to obtain Compound 1b (232 mg, 20%) as a white foam.

後処理

  1. additionwas added dropwise under ice-
  2. temperaturecooling
  3. temperaturewhile refluxing
  4. temperatureunder heating for 3.5 hours
  5. temperatureto cool
  6. washThe organic layer was washed three times with water
  7. dry with materialonce with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate
  8. distillationThe solvent was distilled off
  9. customthe residue was purified by neutral silica gel column chromatography (5% ethyl acetate/n-hexane)

出典と根拠

ORDレコード
ord-cf62d2e8f9544323a2b440b5956b3cc9
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07855300B2

反応ノート

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