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Dichloromethane → 1-(4-Dimethylamino-piperidin-1-yl)-2-hydroxy-2,2-di-thiophen-2-ylethanone

HRID 220332
ノート
印刷プレビュー

反応式

HRID 220332 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6](=[O:10])[C:7](O)=[O:8].C(Cl)Cl.C(Cl)(=O)C(Cl)=O.[CH3:20][N:21]([CH3:28])[CH:22]1[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1.CCN(C(C)C)C(C)C.C1COCC1.[S:43]1[CH:47]=[CH:46][CH:45]=[C:44]1[Mg]Br>CN(C1C=CN=CC=1)C.CN(C=O)C>[CH3:20][N:21]([CH3:28])[CH:22]1[CH2:27][CH2:26][N:25]([C:7](=[O:8])[C:6]([OH:10])([C:2]2[S:1][CH:5]=[CH:4][CH:3]=2)[C:44]2[S:43][CH:47]=[CH:46][CH:45]=2)[CH2:24][CH2:23]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

10

反応物 7

HCID 6344DichloromethaneHCID 8028Tetrahydrofuran2 回HCID 65578Oxalyl chlorideHCID 776942-Thiopheneglyoxylic acidHCID 81531DiisopropylethylamineHCID 417391N,N-Dimethylpiperidin-4-amineHCID 178418438HCID 178418438、化合物

生成物 1

HCID 598285271-(4-Dimethylamino-piperidin-1-yl)-2-hydroxy-2,2-di-thiophen-2-ylethanone

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

To a stirred solution of 2-thiopheneglyoxylic acid (1.0 g, 6.4 mmol) in DCM (100 mL, 2 mol), was added oxalyl chloride (596 μL, 7 mmol) and a catalytic amount of DMF. The mixture was stirred for 2 hours and then was cooled at 0° C. in an ice bath. Dimethyl-piperidin-4-ylamine (821 mg, 6.4 mmol), DIPEA (1.7 mL, 9.6 mmol) and DMAP (20 mg, 0.1 mmol) were added, and the mixture was stirred for 2 hours. The solvent was removed under reduced pressure and the crude mixture was then dissolved in DCM (60 mL), washed with a saturated bicarbonate solution (50 mL), and dried over MgSO4. The solvent was removed under reduced pressure and the crude material was then dissolved in THF (50 mL, 0.6 mol) and cooled to 0° C. in an ice bath. To the stirred solution was added 1.0 M thiophen-2-yl magnesium bromide in THF (7.7 mL, 7.7 mmol) was added. The mixture was stirred for 30 minutes, then quenched with a saturated bicarbonate solution (50 mL) and DCM (50 mL). The organic was taken and dried over MgSO4, and the solvent was removed under reduced pressure, to afford the title compound (1.5 g).

後処理

  1. stirringthe mixture was stirred for 2 hours
  2. customThe solvent was removed under reduced pressure
  3. dissolutionthe crude mixture was then dissolved in DCM (60 mL)
  4. washwashed with a saturated bicarbonate solution (50 mL)
  5. dry with materialdried over MgSO4
  6. customThe solvent was removed under reduced pressure
  7. temperaturecooled to 0° C. in an ice bath
  8. additionwas added
  9. stirringThe mixture was stirred for 30 minutes
  10. customquenched with a saturated bicarbonate solution (50 mL) and DCM (50 mL)
  11. dry with materialdried over MgSO4
  12. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-61b81f85042e4cc6a30b78aa8ac3033d
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08202891B2

反応ノート

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