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Sodium Hydroxide → HCID 178465840, 화합물

HRID 1956423
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HRID 1956423 반응식
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[N:12][C:13]=1[CH3:14])[N:10]=[CH:9][C:8]([C:15]([O:17]CC)=[O:16])=[C:7]2[OH:20])[CH3:2].[OH-].[Na+]>O>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[N:12][C:13]=1[CH3:14])[N:10]=[CH:9][C:8]([C:15]([OH:17])=[O:16])=[C:7]2[OH:20])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 178469690Ethyl 6-ethoxy-4-hydroxy-7-methyl-1,8-naphthyridine-3-carboxylate

생성물 1

HCID 178465840HCID 178465840, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of ethyl 6-ethoxy-4-hydroxy-7-methyl-1,8-naphthyridine-3-carboxylate (10.0 g), 5M sodium hydroxide solution (200 ml), IMS (64 ml) and water (64 ml) was boiled under reflux for 2 hours. The mixture was cooled to ambient temperature and then filtered. The residue was dissolved in water, acidified to pH5 with glacial acetic acid and filtered. The residue was triturated with hot IMS, cooled and filtered to give 6-ethoxy-4-hydroxy-7-methyl-1,8-naphthyridine-3-carboxylic acid, m.p. 259°-261° C.

후처리

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  1. temperatureunder reflux for 2 hours
  2. filtrationfiltered
  3. dissolutionThe residue was dissolved in water
  4. filtrationfiltered
  5. customThe residue was triturated with hot IMS
  6. temperaturecooled
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-05f54d0b57cd484ba60a97b16ca7c485
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05780482

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