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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 5-(Aminomethyl)-2-chloropyridine

HRID 249470
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인쇄 미리보기

반응식

HRID 249470 반응식
O.NN.[Cl:4][C:5]1[N:10]=[CH:9][C:8]([CH2:11][N:12]2C(=O)C3=CC=CC=C3C2=O)=[CH:7][CH:6]=1.O>CCO>[Cl:4][C:5]1[N:10]=[CH:9][C:8]([CH2:11][NH2:12])=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 24654Hydrazine hydrate (1:1)HCID 143247132-[(6-Chloropyridin-3-yl)methyl]-1H-isoindole-1,3(2H)-dione

생성물 1

HCID 70209275-(Aminomethyl)-2-chloropyridine수율 70.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Hydrazine hydrate (1.7 ml) was added to a refluxing solution of 6.5 g (2.4×10-2 mole) of N-(6-chloro-3-pyridylmethyl)phthalimide in 100 ml of EtOH, and the mixture was further refluxed for 1 hour. After addition of 20 ml of water, the ethanol was distilled off under reduced pressure. Concentrated hydrochloric acid (25 ml) was added to the residue and the mixture was refluxed for 1 hour. After cooling, the reaction mixture was neutralized with NaOH and the aqueous layer was saturated with NaCl and extracted with Et2O. The extract was dried over Na2SO4 and the solvent was distilled off to give 2.4 g of the title compound as a yellow oil.

후처리

  1. temperaturethe mixture was further refluxed for 1 hour
  2. distillationthe ethanol was distilled off under reduced pressure
  3. additionConcentrated hydrochloric acid (25 ml) was added to the residue
  4. temperaturethe mixture was refluxed for 1 hour
  5. temperatureAfter cooling
  6. extractionextracted with Et2O
  7. dry with materialThe extract was dried over Na2SO4
  8. distillationthe solvent was distilled off

출처 및 근거

ORD 기록
ord-cee9b61658ec4993a5facdf399428873
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05214152

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