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Hydrochloric Acid → 2-(2-Amino-4-methyl-pentylamino)-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide dihydrochloride

HRID 278895
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HRID 278895 반응식
C(OC(=O)[NH:7][CH:8]([CH2:13][NH:14][CH:15]([C:31](=[O:37])[NH:32][C:33]([CH3:36])([CH3:35])[CH3:34])[CH2:16][C:17]1[CH:22]=[CH:21][C:20]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:19][CH:18]=1)[CH2:9][CH:10]([CH3:12])[CH3:11])(C)(C)C.FC(F)(F)C(O)=O.[ClH:46]>C(Cl)Cl.C(OCC)C>[ClH:46].[ClH:46].[NH2:7][CH:8]([CH2:9][CH:10]([CH3:12])[CH3:11])[CH2:13][NH:14][CH:15]([CH2:16][C:17]1[CH:18]=[CH:19][C:20]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:21][CH:22]=1)[C:31]([NH:32][C:33]([CH3:34])([CH3:35])[CH3:36])=[O:37]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 6422Trifluoroacetic acidHCID 18711794(1-{[2-(4-Benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethylamino]-methyl}-3-methyl-butyl)-carbamic acid tert-butyl ester

생성물 1

HCID 226238692-(2-Amino-4-methyl-pentylamino)-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide dihydrochloride수율 59%

시약·촉매·용매 2

HCID 3283
Diethyl Ether
용매
2회
HCID 6344Dichloromethane용매2회

실험 절차

To a solution of (1-{[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethylamino]-methyl}-3-methyl-butyl)-carbamic acid tert-butyl ester (0.4 g, 0.76 mmol, Example 8, Step A) in CH2Cl2 (7.5 mL) was added trifluoroacetic acid (2.5 mL) at ambient temperature under nitrogen atmosphere. The resulting reaction mixture was stirred for 25 minutes, then concentrated in vacuo. The viscous oil obtained was dissolved in 40 mL of CH2Cl2 and successively washed with saturated aqueous NaHCO3 solution (2×40 mL), brine (2×40 mL), and was dried over Na2SO4. The CH2Cl2 solution of free amine was concentrated in vacuo to afford the crude product as a viscous oil which was then dissolved in 10 mL of ethyl ether. To this solution was added saturated HCl solution in ethyl ether until no more white precipitate formed. Filtration and drying overnight under vacuum afforded 0.15 g (59%) of titled compound as a yellow solid; mp 228-230° C.

후처리

  1. customThe resulting reaction mixture
  2. concentrationconcentrated in vacuo
  3. customThe viscous oil obtained
  4. washsuccessively washed with saturated aqueous NaHCO3 solution (2×40 mL), brine (2×40 mL)
  5. dry with materialwas dried over Na2SO4
  6. concentrationThe CH2Cl2 solution of free amine was concentrated in vacuo
  7. customto afford the crude product as a viscous oil which
  8. customformed
  9. filtrationFiltration
  10. customdrying overnight under vacuum

출처 및 근거

ORD 기록
ord-8b4375fe7ee043bdb7322691f7b510d5
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06362174B1

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