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Sulfuric Acid → (S)-3-Amino-1,2,3,4-tetrahydroquinoline-6-carbonitrile

HRID 1643862
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HRID 1643862 반응식
[C:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[NH:9][CH2:8][C@@H:7]([NH:13]C(=O)[C@@H](O)C1C=CC=CC=1)[CH2:6]2)#[N:2].S(=O)(=O)(O)O>CCO>[NH2:13][C@H:7]1[CH2:6][C:5]2[C:10](=[CH:11][CH:12]=[C:3]([C:1]#[N:2])[CH:4]=2)[NH:9][CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

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HCID 1118Sulfuric AcidHCID 66757271(S)-N-((S)-6-Cyano-1,2,3,4-tetrahydroquinolin-3-yl)-2-hydroxy-2-phenylacetamide

생성물 1

HCID 66757521(S)-3-Amino-1,2,3,4-tetrahydroquinoline-6-carbonitrile수율 73%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 1E (2.5 g, 8.14 mmol) in EtOH (25 mL) was added 15% aqueous sulfuric acid (25 mL). The resulting mixture was refluxed overnight, then cooled to RT. After removal of most of the EtOH, the mixture was diluted with water (200 mL), extracted with CH2Cl2 (3×50 mL). The aqueous layer was basified with 4N NaOH to pH=10, then extracted with CH2Cl2 (3×50 mL). The combined organics were washed with brine, dried (Na2SO4) and concentrated. The residue was crystallized from EtOAc/hexane to afford the title compound (1.026 g, 73% yield).

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후처리

  1. temperatureThe resulting mixture was refluxed overnight
  2. customAfter removal of most of the EtOH
  3. additionthe mixture was diluted with water (200 mL)
  4. extractionextracted with CH2Cl2 (3×50 mL)
  5. extractionextracted with CH2Cl2 (3×50 mL)
  6. washThe combined organics were washed with brine
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated
  9. customThe residue was crystallized from EtOAc/hexane

출처 및 근거

ORD 기록
ord-dfe5bb16074649df984fca84fc45d18c
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08119808B2

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