Hydrochloric Acid → 4-Bromo-6-methoxy-1,5-naphthyridine-3-carboxylic acid

HRID 1441247노트

반응식

HRID 1441247 반응식
[OH-].[Na+].C([O:5][C:6]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[Br:18])=[N:15][C:14]([O:19][CH3:20])=[CH:13][CH:12]=2)=[O:7])C.Cl>C1COCC1>[Br:18][C:17]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([O:19][CH3:20])[N:15]=2)[N:10]=[CH:9][C:8]=1[C:6]([OH:7])=[O:5]

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 68454651Ethyl 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate

생성물 1

HCID 675490654-Bromo-6-methoxy-1,5-naphthyridine-3-carboxylic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

2 N NaOH (300 mL, 600 mmole) was added dropwise over 30 min to a stirred solution of 4-bromo-6-methoxy-[1,5]naphthyridine-3-carboxylic acid ethyl ester (83.56 g, 268 mmole) in THF (835 mL). Stirring was continued overnight, at which time LC/MS showed that the saponification was complete. 2 N HCl was added to pH 6 and the THF was removed in vacuo. 2 N HCl was added to pH 2, then water (250 mL) was added, and the mixture was cooled thoroughly in ice. The solid was collected by suction filtration, washed with water and dried (first using a rotary evaporator at 50° C. and then under high vacuum at 50° C. overnight) to give the title compound (76.7 g, slightly over quantitative). This material was used without further purification.

후처리

  1. customthe THF was removed in vacuo
  2. addition2 N HCl was added to pH 2
  3. additionwater (250 mL) was added
  4. temperaturethe mixture was cooled thoroughly in ice
  5. filtrationThe solid was collected by suction filtration
  6. washwashed with water
  7. customdried (
  8. customa rotary evaporator at 50° C.

출처 및 근거

ORD 기록
ord-2db9bd756a254b1fa1c593605383ec97
출처 데이터셋
uspto-grants-2010_02
특허 번호
US07655648B2

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