Phosphorus oxychloride → Ethyl 6-bromo-4-chloroquinoline-3-carboxylate

HRID 1042325노트

반응식

HRID 1042325 반응식
C(O[C:4](=O)[C:5](=[CH:11][NH:12][C:13]1[CH:18]=[CH:17][C:16]([Br:19])=[CH:15][CH:14]=1)[C:6]([O:8][CH2:9][CH3:10])=[O:7])C.O=P(Cl)(Cl)[Cl:23]>>[CH2:9]([O:8][C:6]([C:5]1[CH:11]=[N:12][C:13]2[C:14]([C:4]=1[Cl:23])=[CH:15][C:16]([Br:19])=[CH:17][CH:18]=2)=[O:7])[CH3:10]

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 1591151Diethyl 2-((4-bromophenylamino)methylene)malonate

생성물 1

HCID 2764138Ethyl 6-bromo-4-chloroquinoline-3-carboxylate수율 52.2%

반응 조건

온도
180 °C

실험 절차

A 20 mL microwave vial was charged with 2-[(4-bromo-phenylamino)methylene]malonic acid diethyl ester (1.711 g, 5.0 mmol) and POCl3 (phosphoryl chloride, 10.0 mL, 16.8 g, 109 mmol). The vial was capped and the mixture was microwave heated stepwise up to 180° C. (watching the pressure) over 5 min and then kept at 180° C. for 30 min Excess POCl3 was evaporated and the residue partitioned between CH2Cl2 (40 mL) and 2 N NaOH (aq) (40 mL). The aqueous layer was extracted with CH2Cl2 (2×40 mL). The organic layers were combined, dried with Na2CO3 and evaporated. The residue was purified on column (silica gel, CH2Cl2 as eluent). Pure fractions were pooled, evaporated and the residue dried under vacuum to give 0.821 g (52%) of 6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester. MS (ESI+) m/z 314, 316 (MH+).

후처리

  1. customThe vial was capped
  2. customover 5 min
  3. customExcess POCl3 was evaporated
  4. customthe residue partitioned between CH2Cl2 (40 mL) and 2 N NaOH (aq) (40 mL)
  5. extractionThe aqueous layer was extracted with CH2Cl2 (2×40 mL)
  6. dry with materialdried with Na2CO3
  7. customevaporated
  8. customThe residue was purified on column (silica gel, CH2Cl2 as eluent)
  9. customevaporated
  10. customthe residue dried under vacuum

출처 및 근거

ORD 기록
ord-1332651a436e490e9980c175c5ffa9f1
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08557843B2

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