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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Butanedioic acid, 2-acetyl-, 1,4-diethyl ester → ethyl (2,6-dimethyl-3H-pyrimidin-4-on-5yl)acetate

HRID 1886056
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반응식

HRID 1886056 반응식
CC[O-].[Na+].Cl.[C:6]([NH2:9])(=[NH:8])[CH3:7].[C:10]([CH:13]([CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:14](OCC)=[O:15])(=O)[CH3:11]>CCO>[CH3:7][C:6]1[NH:9][C:14](=[O:15])[C:13]([CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])=[C:10]([CH3:11])[N:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 66197Butanedioic acid, 2-acetyl-, 1,4-diethyl esterHCID 67170Acetamidine monohydrochlorideHCID 2723922Sodium ethoxide

생성물 1

HCID 135459178ethyl (2,6-dimethyl-3H-pyrimidin-4-on-5yl)acetate수율 27%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of NaOEt (0.069 mol) in EtOH (prepared from 1.6 g of Na in 100 mL of EtOH), acetamidine hydrochloride (6.5 g, 0.069 mol), and diethyl 2-acetylsuccinate (15.0 g, 0.069 mol) was heated under reflux for 16 h. The mixture was concentrated, taken up in water (50 mL), and acidified with 2N HCl (12 mL). The aqueous mixture was extracted with CH2Cl2, and the extracts were dried (MgSO4) and concentrated. Trituration with ether gave 3.9 g (27%) of product as a white solid, mp 175°-177° C.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 16 h
  3. concentrationThe mixture was concentrated
  4. extractionThe aqueous mixture was extracted with CH2Cl2
  5. dry with materialthe extracts were dried (MgSO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-cb767273792f4fc98ce74071b1580e31
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05149699

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