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Hydrochloric Acid → (1S,3S)-N-[2,2-difluoro-2-(4-methylphenyl)ethyl]cyclopentane-1,3-diamine

HRID 271393
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HRID 271393 반응식
B.[NH2:2][C@H:3]1[CH2:7][CH2:6][C@H:5]([NH:8][C:9](=O)[C:10]([F:19])([F:18])[C:11]2[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][CH:12]=2)[CH2:4]1.Cl.C(=O)([O-])[O-].[Na+].[Na+]>C1COCC1>[F:18][C:10]([F:19])([C:11]1[CH:12]=[CH:13][C:14]([CH3:17])=[CH:15][CH:16]=1)[CH2:9][NH:8][C@H:5]1[CH2:6][CH2:7][C@H:3]([NH2:2])[CH2:4]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6331BoraneHCID 10340Sodium CarbonateHCID 59834888N-[(1S,3S)-3-aminocyclopentyl]-2,2-difluoro-2-(4-methylphenyl)acetamide

생성물 1

HCID 58812733(1S,3S)-N-[2,2-difluoro-2-(4-methylphenyl)ethyl]cyclopentane-1,3-diamine수율 65.8%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

1M borane in THF (20 mL, 20 mmol) was added slowly to a stirred solution of N-[(1S,3S)-3-aminocyclopentyl]-2,2-difluoro-2-(4-methylphenyl)acetamide (1.006 g, 3.749 mmol) in dry THF (20 mL) at 0° C. The reaction mixture was warmed to rt. and then was heated to 70° C. for 1 h. The reaction mixture was cooled, quenched with 6N HCl (2.5 mL, 15 mmol) and stirred at rt for 16 h. Aqueous sodium carbonate was added to pH=11, and the mixture was extracted with EtOAc, dried (MgSO4), filtered and concentrated. The resulting oil was purified by silica gel chromatography (eluting with 1.2% NH4OH/10.8% MeOH/CHCl3) to give the title compound as a pale yellow oil (627 mg): MS=255.4 (M+1).

후처리

  1. temperatureand then was heated to 70° C. for 1 h
  2. temperatureThe reaction mixture was cooled
  3. extractionthe mixture was extracted with EtOAc
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe resulting oil was purified by silica gel chromatography (eluting with 1.2% NH4OH/10.8% MeOH/CHCl3)

출처 및 근거

ORD 기록
ord-3ac239e24c7047e699a5a40fd086706f
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452893B2

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