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

HRID 1711194
ノート
印刷プレビュー

反応式

HRID 1711194 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid
溶媒
HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-cf77be83f5d24430af3838ebdf0ec806
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07790747B2

反応ノート

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