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Ethanol → HCID 68533639, 화합물

HRID 2389362
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HRID 2389362 반응식
[C:1]1([CH:7]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:8]2[CH:9]=[CH:10][C:11](=[O:27])[N:12]([CH2:14][CH2:15][N:16]3C(=O)C4C(=CC=CC=4)C3=O)[CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CCO.O.NN>C1COCC1>[NH2:16][CH2:15][CH2:14][N:12]1[CH:13]=[C:8]([CH:7]([C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=2)[C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:9]=[CH:10][C:11]1=[O:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 24654Hydrazine hydrate (1:1)HCID 68533592HCID 68533592, 화합물

생성물 1

HCID 68533639HCID 68533639, 화합물수율 74.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 2-{2-[5-(diphenylmethyl)-2-oxo-1(2H)-pyridinyl]ethyl}-1H-isoindole-1,3(2H)-dione (295 mg) in mixed solvent (EtOH:THF=4.4 mL:2.2 mL) was added hydrazine hydrate (329 μL) and the mixture was stirred at ambient temperature for 1 hour. The resulting mixture was evaporated in vacuo and the residue was diluted with chloroform (10 mL). The mixture was filtered and the filtrate was evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform:MeOH=99:1-96:4) to afford 1-(2-aminoethyl)-5-(diphenylmethyl)-2(1H)-pyridinone (154 mg) as colorless crystals.

후처리

  1. customThe resulting mixture was evaporated in vacuo
  2. additionthe residue was diluted with chloroform (10 mL)
  3. filtrationThe mixture was filtered
  4. customthe filtrate was evaporated in vacuo
  5. customThe residue was purified by silica gel column chromatography (chloroform:MeOH=99:1-96:4)

출처 및 근거

ORD 기록
ord-0fdd8f256ebd445194a2443b885e3da5
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273745B2

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