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Hydrochloric Acid → HCID 59016024, 화합물

HRID 968829
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HRID 968829 반응식
[O-]CC.[Na+].C(OCC)(=O)C.[OH:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][CH2:20][C:21]2[N:22]([CH2:35][CH2:36][CH3:37])[C:23](=[O:34])[N:24]([CH2:26][C:27]3[CH:32]=[CH:31][C:30]([CH3:33])=[CH:29][CH:28]=3)[N:25]=2)=[CH:14][CH:13]=1.[C:38]([O:43][CH:44](CC)[CH2:45]CC)(=[O:42])[CH:39]([CH3:41])[CH3:40].Cl>C(O)C.O.C(OC(CC)CCC)(=O)C(C)C>[CH2:44]([O:43][C:38](=[O:42])[C:39]([CH3:41])([O:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][CH2:20][C:21]2[N:22]([CH2:35][CH2:36][CH3:37])[C:23](=[O:34])[N:24]([CH2:26][C:27]3[CH:28]=[CH:29][C:30]([CH3:33])=[CH:31][CH:32]=3)[N:25]=2)=[CH:14][CH:13]=1)[CH3:40])[CH3:45]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 2723922Sodium ethoxide5회HCID 58579265Ethyl-2-butyl isobutyrate3회HCID 59015891HCID 59015891, 화합물

생성물 1

HCID 59016024HCID 59016024, 화합물수율 63%

시약·촉매·용매 3

HCID 58579265Ethyl-2-butyl isobutyrate촉매HCID 702Ethanol용매HCID 962Water용매

실험 절차

To a mixture of sodium ethoxide (1.22 mL, 3.28 mmol) and ethyl acetate (322 μL, 3.28 mmol) was added 5-[3-(4-hydroxyphenyl)-propyl]-2-(4-methylbenzyl)-4-propyl-2,4-dihydro-[1,2,4]triazol-3-one (1.2 g, 3.28 mmol) in ethanol (10 mL) and the resulting mixture stirred at reflux for 1 hour. Then ethyl-2-butyl isobutyrate (1.08 mL, 7.38 mmol) was added and the reaction continued at reflux for 1 hour. Then sodium ethoxide (1.22 mL, 3.28 mmol) was added dropwise over 5 min and the reaction continued at reflux for 4.5 hour. Additional sodium ethoxide (520 μL, 1.4 mmol) and ethyl-2-butyl isobutyrate (205 μL, 1.4 mmol) were added and reaction continued at reflux for 4 hour. Additional sodium ethoxide (336 μL, 0.903 mmol) and ethyl-2-butyl isobutyrate (132 μL, 0.903 mmol) were added and the reaction continued at reflux for 3 hours. Finally, additional sodium ethoxide (200 μL, 0.54 mmol) and ethyl-2-butyl isobutyrate (100 μL, 0.133 mmol) were added and the reaction continued at reflux for 1.5 hours. The mixture was allowed to cool to room temperature and is then quenched into a solution of conc. HCl (1.5 g, 41 mmol) in water (50 mL). The resulting solution was then concentrated in vacuo, taken up in ethyl acetate (100 mL) and the aqueous layer was discarded. The organic layer was washed with saturated aq. NaHCO3 (2×50 mL) followed by saturated aq. NaCl (2×25 mL). The organic layer was dried (MgSO4), filtered, concentrated, and purified by silica gel chromatography (1:1 ethyl acetate:hexanes) to afford the title compound as a yellow oil (990 mg, 2.06 mmol, 63%):

후처리

  1. temperatureat reflux for 1 hour
  2. temperatureat reflux for 1 hour
  3. temperatureat reflux for 4.5 hour
  4. customreaction
  5. temperatureat reflux for 4 hour
  6. temperatureat reflux for 3 hours
  7. temperatureat reflux for 1.5 hours
  8. concentrationThe resulting solution was then concentrated in vacuo
  9. washThe organic layer was washed with saturated aq. NaHCO3 (2×50 mL)
  10. dry with materialThe organic layer was dried (MgSO4)
  11. filtrationfiltered
  12. concentrationconcentrated
  13. custompurified by silica gel chromatography (1:1 ethyl acetate:hexanes)

출처 및 근거

ORD 기록
ord-678a312068fe442b9c7941984493004d
출처 데이터셋
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07304062B2

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