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Aniline → ((r)-1-Phenylcarbamoyl-butyl)-carbamic acid tert-butyl ester

HRID 1711194
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HRID 1711194 반응식
[C:1]([O:5][C:6]([NH:8][C@H:9]([CH2:13][CH2:14][CH3:15])[C:10]([OH:12])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].CN1CCOCC1.ClC(OCC(C)C)=O.[NH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>C1COCC1.Cl>[C:1]([O:5][C:6](=[O:7])[NH:8][C@@H:9]([C:10](=[O:12])[NH:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[CH2:13][CH2:14][CH3:15])([CH3:2])([CH3:3])[CH3:4]
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참가 물질

7

반응물 4

HCID 6115AnilineHCID 79724-MethylmorpholineHCID 62365Isobutyl chloroformateHCID 6995000(2R)-2-(((tert-butoxy)carbonyl)amino)pentanoic acid

생성물 1

HCID 68777029((r)-1-Phenylcarbamoyl-butyl)-carbamic acid tert-butyl ester

시약·촉매·용매 2

HCID 313Hydrochloric Acid
용매
HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

To a 0° C. solution of the crude carboxylic acid (652 mg, 3.00 mmol) and NMM (0.50 ml, 4.5 mmol) in THF (12 ml) was added isobutyl chloroformate (0.45 ml, 3.5 mmol) and the resulting mixture was stirred at 0° C. for 5 minutes. A solution of aniline (0.45 ml, 4.9 mmol) in THF (3 ml) was then added dropwise. The reaction was warmed to room temperature and stirred for 66 hours. The reaction was diluted with 1M HCl (30 ml) and was extracted with Et2O (25 ml×3). The organic solution was washed with brine (50 ml), was dried (Na2SO4), filtered and concentrated under reduced pressure, giving crude ((R)-1-phenylcarbamoyl-butyl)-carbamic acid tert-butyl ester as an oily, light yellow foam.

후처리

  1. temperatureThe reaction was warmed to room temperature
  2. stirringstirred for 66 hours
  3. extractionwas extracted with Et2O (25 ml×3)
  4. washThe organic solution was washed with brine (50 ml)
  5. dry with materialwas dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-cf77be83f5d24430af3838ebdf0ec806
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07790747B2

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