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Sodium Carbonate → HCID 44517832、化合物

HRID 1951122
ノート
印刷プレビュー

反応式

HRID 1951122 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:12][N:11]([C:13]([CH:15]3[CH2:20][CH2:19][N:18]([CH2:21][CH2:22][CH2:23]SC)[CH2:17][CH2:16]3)=[O:14])[CH2:10][CH:9]2[N:26]([CH3:41])[C:27](=[O:40])[C:28]2[CH:33]=[CH:32][C:31]([O:34][CH3:35])=[C:30]([C:36]([F:39])([F:38])[F:37])[CH:29]=2)=[CH:4][CH:3]=1.Cl[C:43]1C=CC=C(C(OO)=O)C=1.[S:53](=[O:57])(=O)(O)[O-:54].[Na+].C(=O)([O-])[O-].[Na+].[Na+]>ClCCl.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:12][N:11]([C:13]([CH:15]3[CH2:16][CH2:17][N:18]([CH2:21][CH2:22][CH2:23][S:53]([CH3:43])(=[O:57])=[O:54])[CH2:19][CH2:20]3)=[O:14])[CH2:10][CH:9]2[N:26]([CH3:41])[C:27](=[O:40])[C:28]2[CH:33]=[CH:32][C:31]([O:34][CH3:35])=[C:30]([C:36]([F:37])([F:39])[F:38])[CH:29]=2)=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 10340Sodium CarbonateHCID 70297m-Chloroperbenzoic acidHCID 516919Sodium BisulfateHCID 67025603HCID 67025603、化合物

生成物 1

HCID 44517832HCID 44517832、化合物収率 83%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6344Dichloromethane溶媒

実験手順

To a solution of N-{(3RS,4SR)-4-(4-chloro-phenyl)-1-[1-(3-methylsulfanyl-propyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-methoxy-N-methyl-3-trifluoromethyl-benzamide (80 mg, 0.13 mmol) in dichloromethane (2 mL) was added under an atmosphere of nitrogen m-chloroperbenzoic acid (47 mg, 0.27 mmol) and stirred for 3 d at ambient temperature. Further addition of m-chloroperbenzoic acid (47 mg, 0.27 mmol) was followed by stirring for 3 h at ambient temperature. After the addition of an aqueous saturated solution of sodium bisulfate (10 mL) and water (10 mL) it was stirred for 1 h at ambient temperature. The reaction mixture was basified by addition of an aqueous solution of sodium carbonate (1 M). The aqueous layer was extracted with dichloromethane (20 mL) and the organic layers were washed with water (15 mL) and dried over sodium sulfate. Purification by chromatography (SiO2, heptane:(ethyl acetate:triethylamine=95:5):methanol=20:80:0 to 0:85:15) afforded the title compound (70 mg, 83%) as a light brown oil. MS m/e: 644.2 [M]+.

後処理

  1. stirringby stirring for 3 h at ambient temperature
  2. stirringwas stirred for 1 h at ambient temperature
  3. extractionThe aqueous layer was extracted with dichloromethane (20 mL)
  4. washthe organic layers were washed with water (15 mL)
  5. dry with materialdried over sodium sulfate
  6. customPurification by chromatography (SiO2, heptane:(ethyl acetate:triethylamine=95:5):methanol=20:80:0 to 0:85:15)

出典と根拠

ORDレコード
ord-5ef31a8228e74b8485b2fbde7fa65ca5
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08404679B2

反応ノート

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