N-bromobutanimide → (3R,4S)-4-{(2S)-2-benzyloxycarbonylaminopropionyloxy}-3-bromo-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile

HRID 704775

反応式

HRID 704775 の反応式
[Br:1]N1C(=O)CCC1=O.[CH3:9][C:10]1([CH3:22])[CH:15]=[CH:14][C:13]2[CH:16]=[C:17]([C:20]#[N:21])[CH:18]=[CH:19][C:12]=2[O:11]1.[CH2:23]([O:30][C:31]([NH:33][C@H:34]([C:36]([OH:38])=[O:37])[CH3:35])=[O:32])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl>[CH2:23]([O:30][C:31]([NH:33][C@@H:34]([CH3:35])[C:36]([O:38][C@H:14]1[C:13]2[CH:16]=[C:17]([C:20]#[N:21])[CH:18]=[CH:19][C:12]=2[O:11][C:10]([CH3:22])([CH3:9])[C@@H:15]1[Br:1])=[O:37])=[O:32])[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1

参加物

6

反応物 4

HCID 67184N-bromobutanimideHCID 516892Sodium BicarbonateHCID 736104N-carbobenzyloxyalanineHCID 27790742,2-dimethyl-2H-1-benzopyran-6-carbonitrile

生成物 1

HCID 18643511(3R,4S)-4-{(2S)-2-benzyloxycarbonylaminopropionyloxy}-3-bromo-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile収率 29.2%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

N-Bromosuccinimide (6.408 g) was added to a solution of 2,2-dimethyl-2H-1-benzopyran-6-carbonitrile (5.55 g) and N-benzyloxycarbonyl-L-alanine (6.69 g) in chloroform (60 ml). After being stirred under reflux for 16 hours, the mixture was poured into saturated aqueous sodium bicarbonate and diluted with chloroform. The organic layer was separated, washed successively with 5% aqueous sodium thiosulfate, water, and brine, dried over magnesium sulfate, and evaporated in vacuo. The oily residue was dissolved in diisopropyl ether and allowed to stand at ambient temperature. The resulting precipitates were collected by filtration, washed with diisopropyl ether, and dried to give (3R,4S)-4-{(2S)-2-benzyloxycarbonylaminopropionyloxy}-3-bromo-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile (4.26 g).

後処理

  1. temperatureunder reflux for 16 hours
  2. customThe organic layer was separated
  3. washwashed successively with 5% aqueous sodium thiosulfate, water, and brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated in vacuo
  6. dissolutionThe oily residue was dissolved in diisopropyl ether
  7. customto stand at ambient temperature
  8. customThe resulting precipitates
  9. filtrationwere collected by filtration
  10. washwashed with diisopropyl ether
  11. customdried

出典と根拠

ORDレコード
ord-cb274ed93a204a2890355bd1365967bf
出典データセット
uspto-grants-1991_01
特許番号
US04988723

関連ノート

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