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Ethyl 2-(6-aminopyridin-3-yl)acetate → Benzyl 2-(6-aminopyridin-3-yl)acetate

HRID 655676
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HRID 655676 반응식
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:4][CH:3]=1>C(O)C1C=CC=CC=1.[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC>[NH2:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][C:9]([O:11][CH2:12][C:13]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[O:10])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 67143734Ethyl 2-(6-aminopyridin-3-yl)acetate

생성물 1

HCID 59411185Benzyl 2-(6-aminopyridin-3-yl)acetate

시약·촉매·용매 2

HCID 76524Titanium tetraethoxide촉매HCID 244Benzyl Alcohol용매

반응 조건

온도
110 °C

실험 절차

Ethyl 2-(6-aminopyridin-3-yl)acetate (described in WO 2009/091014) (1.5 g) was dissolved in benzyl alcohol (10 mL). Titanium(IV) ethoxide (1.74 mL) was added and the reaction was heated to 110° C. for 16 hours. The reaction was cooled to room temperature and quenched with 1N HCl. This mixture was basified with saturated sodium bicarbonate and extracted three times with ethyl acetate. The combined organics were dried over MgSO4, filtered, and concentrated. Purification by column chromatography, eluting with a gradient of 30-100% ethyl acetate in heptane, afforded the title compound Intermediate (5b) (1.04 g, 51% yield) as a white solid. 1H NMR (400 MHz, CDCl3) δ 3.51 (2 H), 4.37 (2 H), 5.11 (2 H), 6.46 (1 H), 7.27-7.41 (6 H), 7.95 (1H). m/z 243.4 (M+H)+.

후처리

  1. temperatureThe reaction was cooled to room temperature
  2. customquenched with 1N HCl
  3. extractionextracted three times with ethyl acetate
  4. dry with materialThe combined organics were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customPurification by column chromatography
  8. washeluting with a gradient of 30-100% ethyl acetate in heptane

출처 및 근거

ORD 기록
ord-4da6d4af34914f82bf8f84ee13483b86
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071606B2

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