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Phosphorus oxychloride → Ethyl 4-chloro-6-methoxyquinoline-3-carboxylate

HRID 495466
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HRID 495466 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[CH:8][C:7]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[C:6]2O.O=P(Cl)(Cl)[Cl:21].P(Cl)(Cl)(Cl)(Cl)Cl>C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[CH:8][C:7]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[C:6]2[Cl:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 178469588HCID 178469588, 화합물

생성물 1

HCID 304558Ethyl 4-chloro-6-methoxyquinoline-3-carboxylate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a stirred solution of the crude 6-methoxy-4-hydroxy-3-ethoxycarbonylquinoline (Step A, 74 g, 0.25 M) in dry toluene (300 mL) was added POCl3 (46.6 mL, 0.5 mol) followed by PCl5 (26 g, 0.125 mol). The mixture was heated at reflux for 6 h. The toluene and the excess of POCl3 were removed under vacuum. The solid residue was suspended into a mixture of 1N NaOH and ice. The resulting solid was filtered off, washed several times with water, then with a minimum amount of MeOH, and dried over P2O5 to give 6-methoxy-4-chloro-3-ethoxycarbonylquinoline as a white solid.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 6 h
  3. customThe toluene and the excess of POCl3 were removed under vacuum
  4. additionThe solid residue was suspended into a mixture of 1N NaOH and ice
  5. filtrationThe resulting solid was filtered off
  6. washwashed several times with water
  7. dry with materialwith a minimum amount of MeOH, and dried over P2O5

출처 및 근거

ORD 기록
ord-1730f8fe5bb944a8ac2c86950b4070b0
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06939874B2

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