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1,2-Dichloroethane → 4-[4-(1-Oxo-but-2-ynylamino)-benzenesulfonyl]-piperazine-1-carboxylic acid tert-butyl ester

HRID 1841918
ノート
印刷プレビュー

反応式

HRID 1841918 の反応式
[C:1]([OH:6])(=O)[C:2]#[C:3][CH3:4].N1C=CC=CC=1.[C:13]([O:17][C:18]([N:20]1[CH2:25][CH2:24][N:23]([S:26]([C:29]2[CH:34]=[CH:33][C:32]([NH2:35])=[CH:31][CH:30]=2)(=[O:28])=[O:27])[CH2:22][CH2:21]1)=[O:19])([CH3:16])([CH3:15])[CH3:14].C(Cl)CCl>C1COCC1.CC(N(C)C)=O.C(OCC)(=O)C>[C:13]([O:17][C:18]([N:20]1[CH2:25][CH2:24][N:23]([S:26]([C:29]2[CH:30]=[CH:31][C:32]([NH:35][C:1](=[O:6])[C:2]#[C:3][CH3:4])=[CH:33][CH:34]=2)(=[O:28])=[O:27])[CH2:22][CH2:21]1)=[O:19])([CH3:16])([CH3:14])[CH3:15]
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 111,2-DichloroethaneHCID 1049PyridineHCID 685352-Butynoic acidHCID 10617209tert-Butyl 4-(4-aminophenylsulfonyl)piperazine-1-carboxylate

生成物 1

HCID 569547204-[4-(1-Oxo-but-2-ynylamino)-benzenesulfonyl]-piperazine-1-carboxylic acid tert-butyl ester収率 20.8%

試薬・触媒・溶媒 2

HCID 8857
Ethyl Acetate
溶媒
HCID 69293768tetrahydrofuran N,N-dimethylacetamide溶媒

実験手順

But-2-ynoic acid (0.19 g, 2.36 mmol) followed by pyridine (0.6 ml), were added sequentially portion wise to a stirred solution of 4-(4-amino-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butyl ester (0.2 g, 0.59 mmol) in THF/DMA (3:2, 5 ml) at room temperature. To this mixture was added EDC (0.6 g, 3.1 mmol) in one portion and the mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. After this time the mixture was diluted with ethyl acetate (50 ml) and washed with water (100 ml), saturated NaHCO3 (100 ml) and HCl (100 ml, 2M). The organic layer was separated, dried (MgSO4), filtered and concentrated under vacuum and the resulting residue was purified by flash column chromatography (elution, 20% ethyl acetate, 80% DCM) to give the title compound (0.05 g, 19% yield) as a white solid. Tr=4.12 min, m/z (ES+) (M+Na)+ 430.

後処理

  1. washwashed with water (100 ml), saturated NaHCO3 (100 ml) and HCl (100 ml, 2M)
  2. customThe organic layer was separated
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum
  6. customthe resulting residue was purified by flash column chromatography (elution, 20% ethyl acetate, 80% DCM)

出典と根拠

ORDレコード
ord-c8e797c64b3f47c9883cc0d88d728f0a
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08946197B2

反応ノート

読み込み中…

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