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Ethyl Acetate → HCID 58387955, 화합물

HRID 2079953
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HRID 2079953 반응식
[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[CH:11][O:12]CC)=[N:6][C:5]=1[NH2:15].C(=O)(O)[O-].[Na+].[BH4-].[Na+].C(OCC)(=O)C>Cl.C(O)C.O1CCCC1>[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][OH:12])=[N:6][C:5]=1[NH2:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 8857Ethyl AcetateHCID 516892Sodium BicarbonateHCID 4311764Sodium borohydrideHCID 67119555HCID 67119555, 화합물

생성물 1

HCID 58387955HCID 58387955, 화합물수율 40%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매
HCID 702
Ethanol
용매
HCID 8028Tetrahydrofuran용매

실험 절차

2-Amino-6-(2-ethoxy-vinyl)-nicotinic acid methyl ester (1.07 g, 4.81 mmol) was dissolved in 5N-hydrochloric acid (25 mL), ethanol (20 mL) and tetrahydrofuran (5 mL), and the solution was stirred for 3 hours under reflux. This reaction mixture was allowed to room temperature, and neutralized with a aqueous solution of saturated sodium bicarbonate, then, sodium borohydride (1 g, 26.5 mmol) was added to this reaction mixture, which was then stirred for 20 minutes at room temperature. Ethyl acetate was added thereto, followed by filtrating through Celite pad. This filtrate was partitioned. This organic layer was separated, the solvent was evaporated in vacuo, the residue was purified by silica gel column chromatography, and the title compound (350 mg, 1.92 mmol, 40%) was obtained as a brown oil.

후처리

  1. temperatureunder reflux
  2. customwas allowed to room temperature
  3. stirringwas then stirred for 20 minutes at room temperature
  4. filtrationby filtrating through Celite pad
  5. customThis filtrate was partitioned
  6. customThis organic layer was separated
  7. customthe solvent was evaporated in vacuo
  8. customthe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-7303963a86174f958ed1843efbb8f200
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932272B2

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