Dimethylformamide → HCID 9904333, 화합물

HRID 1279235노트

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HRID 1279235 반응식
[NH:1]1[CH:6]=[C:5]([C:7]([OH:9])=O)[C:4](=[O:10])[C:3]2[CH2:11][CH2:12][CH2:13][C:2]1=2.CN(C=O)C.ClC(OCC)=O.[CH3:25][O:26][C:27]1[CH:34]=[CH:33][C:30]([CH2:31][NH2:32])=[CH:29][CH:28]=1>C1COCC1.O>[CH3:25][O:26][C:27]1[CH:34]=[CH:33][C:30]([CH2:31][NH:32][C:7]([C:5]2[C:4](=[O:10])[C:3]3[CH2:11][CH2:12][CH2:13][C:2]=3[NH:1][CH:6]=2)=[O:9])=[CH:29][CH:28]=1

참가 물질

7

반응물 4

HCID 6228DimethylformamideHCID 10928Ethyl chloroformateHCID 754524-MethoxybenzylamineHCID 122914536,7-Dihydro-4-hydroxy-5H-cyclopenta[b]pyridine-3-carboxylic acid

생성물 1

HCID 9904333HCID 9904333, 화합물수율 48.9%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

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온도
90 °C

실험 절차

A quantity of 100 mg (0.61 mmole, 1.0 eq) of 4,5,6,7-tetrahydro-1H-cyclopenta[b]pyridin-4-one-3-carboxylic acid is dissolved in 5 mL THF and 1 mL DMF and treated at 0° C. with 0.18 mL (1.2 mmole, 2.2 eq) TEA followed by 0.12 mL (1.2 mmole, 2.2 eq) of ethyl chloroformate. The resulting solution is stirred for 30 min. at which time 0.17 mL (1.2 mmole, 2.2 eq) of 4-methoxybenzylamine is added. The solution is allowed to warm to room temperature for 1 hr before the addition of 20 mL of H2O, the THF is removed under reduced pressure, and the resulting solid is filtered and washed with H2O and then Et2O. The resulting solid is slurried in 1 mL EtOH and 5 mL 10% NaOH, warmed to 90° C. for 10 min., cooled to 0° C., and pH adjusted to 9.0 with 3N HC1. The resulting solid is filtered, washed with H2O, Et2O, and purified by chromatography (silica gel, 10% CH3OH/ CH2Cl2), to yield 89 mg of N-(4-Methoxybenzyl)-4,5,6,7-tetrahydro-1H-cyclopenta[b]pyridin-4-one-3-carboxamide (compound 1), mp 240-241° C.

후처리

  1. additionis added
  2. customthe THF is removed under reduced pressure
  3. filtrationthe resulting solid is filtered
  4. washwashed with H2O
  5. temperaturecooled to 0° C.
  6. filtrationThe resulting solid is filtered
  7. washwashed with H2O, Et2O
  8. custompurified by chromatography (silica gel, 10% CH3OH/ CH2Cl2)

출처 및 근거

ORD 기록
ord-0997da7128fa4abf859cdb9fae6ab4ea
출처 데이터셋
uspto-grants-2002_09
특허 번호
US06448259B1

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