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Hydrochloric Acid → N-{(1S,2R)-1-(3,5-Difluorobenzyl)-2-hydroxy-3-[(6-neopentyl-1,2,3,4-tetrahydroquinolin-4-YL)amino]propyl}acetamide

HRID 1991552
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HRID 1991552 반응식
[C:1]([NH:4][C@@H:5]([CH2:35][C:36]1[CH:41]=[C:40]([F:42])[CH:39]=[C:38]([F:43])[CH:37]=1)[C@H:6]([OH:34])[CH2:7][NH:8][CH:9]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([CH2:19][C:20]([CH3:23])([CH3:22])[CH3:21])[CH:17]=2)[N:12](C(OCC2C=CC=CC=2)=O)[CH2:11][CH2:10]1)(=[O:3])[CH3:2].Cl>CCO.[Pd]>[F:42][C:40]1[CH:41]=[C:36]([CH:37]=[C:38]([F:43])[CH:39]=1)[CH2:35][C@H:5]([NH:4][C:1](=[O:3])[CH3:2])[C@H:6]([OH:34])[CH2:7][NH:8][CH:9]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([CH2:19][C:20]([CH3:23])([CH3:22])[CH3:21])[CH:17]=2)[NH:12][CH2:11][CH2:10]1
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 58909414HCID 58909414, 화합물

생성물 1

HCID 10411894N-{(1S,2R)-1-(3,5-Difluorobenzyl)-2-hydroxy-3-[(6-neopentyl-1,2,3,4-tetrahydroquinolin-4-YL)amino]propyl}acetamide수율 50.7%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a solution of benzyl 4-{[(2R,3S)-3-(acetylamino)-4-(3,5-difluorophenyl)-2-hydroxybutyl]amino}-6-neopentyl-3,4-dihydroquinoline-1(2H)-carboxylate (0.242 g) in EtOH (30 mL) was added 1N HCl (1.0 mL) and 10% palladium on carbon (0.030 g). The mixture was degassed with N2 for five minutes. The mixture was placed on a hydrogenation apparatus under 47 psi of H2 and was shaken for 4.5 hours. The palladium was filtered off using Celite and the solvent was concentrated under reduced pressure. The residue was then partitioned between water and ethyl acetate and the organic layers were washed with aqueous sodium bicarbonate, dried with magnesium sulfate, filtered, and concentrated. A silica gel column using 4% MeOH in dichloromethane with 0.25% NH4OH as the solvent solution gave 0.095 g of the title compound. MS (ESI+) for C26H35F2N3O2 m/z 460.27 (M+H)+.

후처리

  1. customThe mixture was degassed with N2 for five minutes
  2. filtrationThe palladium was filtered off
  3. concentrationthe solvent was concentrated under reduced pressure
  4. customThe residue was then partitioned between water and ethyl acetate
  5. washthe organic layers were washed with aqueous sodium bicarbonate
  6. dry with materialdried with magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-af9336227c454c8daa107dc53afc4239
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07645780B2

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