Ethylmorpholine → HCID 86628722、化合物

HRID 1071693

反応式

HRID 1071693 の反応式
[C:1]([O:5][C:6]([CH2:8][N:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[C:10]1[C:18](O)=[O:19])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N1CCOCC1)C.Cl.[CH:30]([N:33]1[CH2:38][CH2:37][CH:36]([NH2:39])[CH2:35][CH2:34]1)([CH3:32])[CH3:31]>ClCCl>[CH:30]([N:33]1[CH2:38][CH2:37][CH:36]([NH:39][C:18]([C:10]2[N:9]([CH2:8][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C:17]3[C:12]([CH:11]=2)=[CH:13][CH:14]=[CH:15][CH:16]=3)=[O:19])[CH2:35][CH2:34]1)([CH3:32])[CH3:31]

参加物

5

反応物 3

HCID 7525EthylmorpholineHCID 21749024N-(tert-butoxycarbonylmethyl)-2-indolecarboxylic acidHCID 230334601-Isopropylpiperidin-4-amine hydrochloride

生成物 1

HCID 86628722HCID 86628722、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 0.5 g 1-tert.-butoxycarbonylmethyl-1H-indole-2-carboxylic acid and 0.91 ml N-ethylmorpholine in 3 ml dichloromethane 0.6 g O-[(ethoxycarbonyl)cyanomethylenamino]-N,N,N′,N′-tetramethyluronium tetrafluoroborate were added and the mixture was stirred for 30 min at room temperature. 0.39 g 1-isopropyl-piperidin-4-ylamine hydrochloride were added to the mixture and the reaction mixture was further stirred for 1 hour. After removal of the solvent under reduced pressure the residue was partitioned between 15 ml water and 15 ml dichloromethane. The organic layer was washed with additional water and then dried over sodium sulphate. After filtration the solvent was removed under reduced pressure and a white solid was obtained. The residue was directly subjected to the subsequent reaction without further purification.

後処理

  1. stirringthe reaction mixture was further stirred for 1 hour
  2. customAfter removal of the solvent under reduced pressure the residue
  3. customwas partitioned between 15 ml water and 15 ml dichloromethane
  4. washThe organic layer was washed with additional water
  5. dry with materialdried over sodium sulphate
  6. filtrationAfter filtration the solvent
  7. customwas removed under reduced pressure
  8. customa white solid was obtained
  9. customThe residue was directly subjected to the subsequent reaction without further purification

出典と根拠

ORDレコード
ord-37a5fa146fd443cfb9fd198d77a370cf
出典データセット
uspto-grants-2005_06
特許番号
US06906084B2

関連ノート

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