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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Methanol → HCID 22747784、化合物

HRID 1641594
ノート
印刷プレビュー

反応式

HRID 1641594 の反応式
C([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]([N:14]2[CH2:19][CH2:18][CH:17]([NH:20][S:21]([C:23]([CH3:26])([CH3:25])[CH3:24])=[O:22])[CH2:16][CH2:15]2)=[O:13])=[CH:7][CH:6]=1)(C)(C)C.[CH:27]1[CH:32]=C(C([O-])=O)C(C(O[O-])=O)=[CH:29][CH:28]=1.[Mg+2].C[OH:42]>C(Cl)Cl.O>[CH2:32]([C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12]([N:14]2[CH2:19][CH2:18][CH:17]([NH:20][S:21]([C:23]([CH3:24])([CH3:25])[CH3:26])(=[O:42])=[O:22])[CH2:16][CH2:15]2)=[O:13])=[CH:9][CH:10]=1)[CH2:27][CH2:28][CH3:29]
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 3

HCID 887MethanolHCID 10130449Monoperoxyphthalic Acid Magnesium SaltHCID 66739112HCID 66739112、化合物

生成物 1

HCID 22747784HCID 22747784、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

実験手順

In a mixture of 2 ml of methanol and 2 ml of methylene chloride, 291 mg of 4-t-butylsulfinylaminopiperidine-1-carboxylic acid(4-t-butylphenyl)amide was dissolved. To the mixture, 570 mg of 80%-MMPP (magnesium monoperoxyphthalate hexahydrate) was added and the mixture was stirred at room temperature for 2 hours. The solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine and dried over magnesium sulfate anhydride. The solvent was removed under reduced pressure and the residue was purified by silica gel chromatography to give 130 mg of 4-t-butylsulfonylaminopiperidine-1-carboxylic acid(4-butylphenyl)amide (I-120).

後処理

  1. dissolutionwas dissolved
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate anhydride
  5. customThe solvent was removed under reduced pressure
  6. customthe residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-35cf59e6d42748dba8317ecb596a1f3b
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08115027B2

反応ノート

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