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4-Methylmorpholine → HCID 57736467、化合物

HRID 1641690
ノート
印刷プレビュー

反応式

HRID 1641690 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:9]([S:20][C:21]1[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=1)C1C(C)=CC(C(O)=O)=NC=1.Cl.CN.ON1C2[CH:37]=[CH:38][CH:39]=CC=2N=N1.C[N:42]1[CH2:47][CH2:46][O:45][CH2:44][CH2:43]1.Cl.C(N=C=NCCC[N:57]([CH3:59])C)C.ClC1C=CC=C(C(OO)=[O:68])C=1>C(Cl)Cl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:9]([S:20]([C:21]1[CH:22]=[CH:23][C:24]([F:27])=[CH:25][CH:26]=1)=[O:68])[C:44]1[C:38]([CH3:39])=[CH:37][C:47]([C:46]([NH:57][CH3:59])=[O:45])=[N:42][CH:43]=1
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 6

HCID 79724-MethylmorpholineHCID 70297m-Chloroperbenzoic acidHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 6364545Methylamine hydrochlorideHCID 57736444HCID 57736444、化合物

生成物 1

HCID 57736467
HCID 57736467、化合物
収率 75.6%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of 5-[(2,5-difluorophenyl) [(4-fluorophenyl)thio]methyl]-4-meth ylpyridine-2-carboxylic acid (307 mg, 0.79 mmol) in methylene chloride (8 ml), methylamine hydrochloride (108 mg, 1.58 mmol), 1-hydroxybenzotriazole (213 mg, 1.58 mmol), 4-methylmorpholine (0.347 ml, 3.15 mmol), and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (302 mg, 1.58 mmol) were added at room temperature. After stirring for 16 hours at room temperature, the reaction mixture was washed with saturated aqueous sodium hydrogencarbonate. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and the resulting residue was subjected to flash silica gel chromatography. The fraction obtained from an elution with hexane:ethyl acetate=3:1 was concentrated under reduced pressure. To a solution of the resulting residue in methylene chloride (5 ml), 3-chloroperbenzoic acid (110 mg, 0.41 mmol) was added at 0° C. After stirring for 1 hour at room temperature, the reaction mixture was washed with 1 N aqueous sodium hydroxide. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and the resulting residue was subjected to preparative thin-layer chromatography (developed with hexane:ethyl acetate=2:1, eluted with methylene chloride:methanol=4:1). The obtained fraction was concentrated under reduced pressure, and the resulting residue was washed with a mixed solvent of ethanol and hexane, and was collected by filtration, to obtain the title compound (129 mg, 0.31 mmol, 39%) as a white solid.

後処理

  1. washthe reaction mixture was washed with saturated aqueous sodium hydrogencarbonate
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customThe fraction obtained from an elution with hexane
  6. concentrationethyl acetate=3:1 was concentrated under reduced pressure
  7. stirringAfter stirring for 1 hour at room temperature
  8. washthe reaction mixture was washed with 1 N aqueous sodium hydroxide
  9. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  10. filtrationfiltered
  11. concentrationthe filtrate was concentrated under reduced pressure
  12. washthin-layer chromatography (developed with hexane:ethyl acetate=2:1, eluted with methylene chloride:methanol=4:1)
  13. concentrationThe obtained fraction was concentrated under reduced pressure
  14. washthe resulting residue was washed with a mixed solvent of ethanol and hexane
  15. filtrationwas collected by filtration

出典と根拠

ORDレコード
ord-187c8815db2d4c5e8f1963a9b209df75
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08114886B2

反応ノート

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