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4-Methylmorpholine → t-butoxycarbonyl-N-(5-methoxy-5-oxopentyl)-L-phenylalaninamide

HRID 3783
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HRID 3783 반응식
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:17]([OH:19])=O)[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CN1CCOCC1.C(OC(Cl)=O)C(C)C.Cl.[NH2:36][CH2:37][CH2:38][CH2:39][CH2:40][C:41]([O:43][CH3:44])=[O:42]>CN(C)C=O>[C:1]([O:5][C:6]([NH:8][C@H:9]([C:17]([NH:36][CH2:37][CH2:38][CH2:39][CH2:40][C:41]([O:43][CH3:44])=[O:42])=[O:19])[CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)=[O:7])([CH3:2])([CH3:3])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 79724-Methylmorpholine2회HCID 62365Isobutyl chloroformateHCID 77857L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 13672034Methyl 5-aminopentanoate hydrochloride

생성물 1

HCID 13385868t-butoxycarbonyl-N-(5-methoxy-5-oxopentyl)-L-phenylalaninamide수율 96.2%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

To a cold (ca -30° ), stirred solution of 26.5 g (0.1 mole) of t-butoxycarbonylphenylalanine (BOC-Phe) and 11.2 g (0.1 mole) of N-methylmorpholine in 150 ml of dimethylformamide (DMF) was added dropwise 13.2 ml (0.1 mole) of isobutylchloroformate. After warming and then holding the temperature at ca. -15° for about ten minutes, the solution was recooled to ca. -39°. To the cold mixture was added additional N-methylmorpholine (12.3 ml, ca. 0.11 mole), followed by 18.5 g (0.11 mole) of methyl 5-aminopentanoate hydrochloride. The mixture was allowed to warm to room temperature and to stand overnight. Solvent and other volatiles were removed by concentration in vacuo. The residue was triturated with ethyl acetate, which was then washed successively with water, 0.5M potassium bisulfate, water, and again with 0.5M potassium bisulfate, and then dried over magnesium sulfate, filtered, and concentrated to a white solid. After collection, the white solid was washed thoroughly with Skellysolve B to give 36.4 g of the title compound, m.p. 98°-100°. Recrystallization from ethyl acetate/Skellysolve B afforded analytically pure crystals.

후처리

  1. temperatureAfter warming
  2. customat ca. -15°
  3. customfor about ten minutes
  4. customwas recooled to ca. -39°
  5. customSolvent and other volatiles were removed by concentration in vacuo
  6. customThe residue was triturated with ethyl acetate, which
  7. washwas then washed successively with water, 0.5M potassium bisulfate, water
  8. dry with materialagain with 0.5M potassium bisulfate, and then dried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated to a white solid
  11. customAfter collection
  12. washthe white solid was washed thoroughly with Skellysolve B

출처 및 근거

ORD 기록
ord-35eabf0f8e394ae3b362808c91e10ea1
출처 데이터셋
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04722922

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