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Methanol → methyl (Z)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-pentenoate

HRID 1780984
ノート
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反応式

HRID 1780984 の反応式
[Cl-].[CH3:2][N:3]([NH+]=CCl)[CH3:4].[O:8]1CCC[CH2:9]1.[NH2:13][C:14]1[S:15][CH:16]=[C:17](/[C:19](=[CH:23]/[CH2:24][CH3:25])/C(O)=O)[N:18]=1.[C:26](=O)([O-])O.[Na+].[CH3:31][OH:32]>>[CH3:2][N:3]([CH:4]=[N:13][C:14]1[S:15][CH:16]=[C:17](/[C:19](=[CH:23]/[CH2:24][CH3:25])/[C:31]([O:8][CH3:9])=[O:32])[N:18]=1)[CH3:26]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 887MethanolHCID 8028TetrahydrofuranHCID 516892Sodium BicarbonateHCID 11344627(Z)-2-(2-Aminothiazol-4-YL)-2-pentenoic acidHCID 86750850Dimethylaminochloromethyleneammonium chloride

生成物 1

HCID 86750854methyl (Z)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-pentenoate収率 67%

実験手順

Dimethylaminochloromethyleneammonium chloride (830 mg, 6.5 mmol) was added to 12 ml of tetrahydrofuran, and the resulting mixture was ice-cooled. Added to the mixture were 196 mg (0.99 mmol) of (Z)-2-(2-aminothiazol-4-yl)-2-pentenoic acid, followed by stirring for 1 hour. Methanol (10 ml) was added thereto. The mixture so obtained was stirred for 30 minutes. The mixture was then poured into 60 ml of a saturated aqueous solution of sodium hydrogencarbonate. The mixture so obtained was extracted three times with 40 ml portions of ethyl acetate. The extract was dried over anhydrous magnesium sulfate and was then filtered. The filtrate was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column, whereby 177 mg of the title compound were obtained (yield: 67%).

後処理

  1. temperaturecooled
  2. additionAdded to the mixture
  3. customThe mixture so obtained
  4. stirringwas stirred for 30 minutes
  5. customThe mixture so obtained
  6. extractionwas extracted three times with 40 ml portions of ethyl acetate
  7. dry with materialThe extract was dried over anhydrous magnesium sulfate
  8. filtrationwas then filtered
  9. concentrationThe filtrate was concentrated under reduced pressure
  10. customThe residue was purified by chromatography on a silica gel column

出典と根拠

ORDレコード
ord-8f24189601874b8dbcf6802f3355fe98
出典データセット
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05631378

反応ノート

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