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Pyridine → HCID 13604836, 화합물

HRID 1708975
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HRID 1708975 반응식
[CH2:1]([NH:3]Cl)[CH3:2].N1C=CC=CC=1.[CH3:11][C@@H:12]1[C@:17]([CH2:19][C:20]2[C:26](=[O:27])[CH:25]=[CH:24][C:22](=[O:23])[CH:21]=2)([CH3:18])[C@@H:16]2[CH2:28][CH2:29][CH:30]=[C:31]([CH3:32])[C@@:15]2([CH3:33])[CH2:14][CH2:13]1>C(O)C>[CH3:2][CH2:1][NH:3][C:24]1[C:22](=[O:23])[CH:21]=[C:20]([CH2:19][C@@:17]2([CH3:18])[C@@H:16]3[CH2:28][CH2:29][CH:30]=[C:31]([CH3:32])[C@@:15]3([CH3:33])[CH2:14][CH2:13][C@@H:12]2[CH3:11])[C:26](=[O:27])[CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 72186AvaroneHCID 12815210N-Ethylhypochlorous amide

생성물 1

HCID 13604836HCID 13604836, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Add 2.5 g of ethylamino hydrochloride and 5 ml of pyridine to a solution of 500 mg avarone in 1000 ml of 50% ethanol, and distill off the ethanol under water-jet vacuum after 20 hours. Extract the aqueous residue with dichloromethane and chromatograph the reduced dichloromethane extract using a silica gel column and dichloromethane as extraction agent. In the course of this process 3'-ethylamino and 4'-ethylamino avarone is obtained.

후처리

  1. distillationdistill off the ethanol under water-jet vacuum after 20 hours
  2. extractionExtract the aqueous residue with dichloromethane and chromatograph the reduced dichloromethane
  3. extractionextract
  4. extractionas extraction agent

출처 및 근거

ORD 기록
ord-bf305ac3dd894bdf8b98e1d57cafaf69
출처 데이터셋
uspto-grants-1990_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04946869

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