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Chloroacetamide → HCID 59854945, 화합물

HRID 2375364
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HRID 2375364 반응식
[C:1]([C:3](=[CH:7][C:8]1[S:9][CH:10]=[CH:11][CH:12]=1)[C:4]([NH2:6])=[S:5])#[N:2].[C:13]([N:20]1[CH2:25][CH2:24][CH2:23][C:22](=O)[CH2:21]1)([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14].N1CCOCC1.Cl[CH2:34][C:35]([NH2:37])=[O:36].C([O-])([O-])=O.[K+].[K+]>C(O)C>[C:16]([O:15][C:13]([N:20]1[CH2:25][C:24]2[N:6]=[C:4]3[S:5][C:34]([C:35](=[O:36])[NH2:37])=[C:1]([NH2:2])[C:3]3=[C:7]([C:8]3[S:9][CH:10]=[CH:11][CH:12]=3)[C:23]=2[CH2:22][CH2:21]1)=[O:14])([CH3:19])([CH3:18])[CH3:17]
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7

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HCID 6580ChloroacetamideHCID 8083MorpholineHCID 11430Potassium CarbonateHCID 27298552-Cyano-3-thiophen-2-yl-thioacrylamideHCID 2756825Tert-butyl 3-oxopiperidine-1-carboxylate

생성물 1

HCID 59854945HCID 59854945, 화합물

시약·촉매·용매 1

HCID 702
Ethanol
용매

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온도
80 °C

실험 절차

To a mixture of 2-cyano-3-thiophen-2-yl-thioacrylamide (4.38 g, 22.5 mmol) and 1-boc-3-piperidone (4.49 g, 22.5 mmol) in 200 ml of anhydrous ethanol was added morpholine (3.94 g, 45 mmol) at room temperature with stirring. The resulting mixture was heated to reflux overnight. Then, 2-chloroacetamide (4.21 g, 45 mmol) and K2CO3 (6.23 g, 45 mmol) was added. The reaction mixture was continued to heat at 80° C. overnight. The solvent was removed in vacuo, and the residue was purified by silica gel column (chloroform/methanol, 40:1) and recrystallized from methanol to give a yellow crystalline product.

후처리

  1. temperatureThe resulting mixture was heated
  2. temperatureto reflux overnight
  3. customThe solvent was removed in vacuo
  4. customthe residue was purified by silica gel column (chloroform/methanol, 40:1)
  5. customrecrystallized from methanol
  6. customto give a yellow crystalline product

출처 및 근거

ORD 기록
ord-70b651da65ca436a89d231c1513c60d7
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07465742B2

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