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Triethylamine → HCID 178485750、化合物

HRID 1031756
ノート
印刷プレビュー

反応式

HRID 1031756 の反応式
[C:1]([O:5][C:6]([NH:8][CH2:9][C@H:10]1[CH2:15][CH2:14][C@H:13]([C:16]([OH:18])=O)[CH2:12][CH2:11]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N(CC)CC)C.C(Cl)(=O)OCC.Cl.[CH3:33][N:34](C)[C:35](=[O:45])[C@H:36]([CH2:38][C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)[NH2:37]>O1CCCC1.CN(C)C=O>[CH3:33][NH:34][C:35](=[O:45])[C@H:36]([CH2:38][C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)[NH:37][C:16]([C@H:13]1[CH2:12][CH2:11][C@H:10]([CH2:9][NH:8][C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH2:15][CH2:14]1)=[O:18]
参加物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 8471Triethylamine2 回HCID 10928Ethyl chloroformateHCID 12653778(2S)-2-Amino-N,N-dimethyl-3-phenylpropanamide hydrochlorideHCID 178453624HCID 178453624、化合物

生成物 1

HCID 178485750HCID 178485750、化合物

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide
溶媒
HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To the compounds (I) (19.15 g) was added dry 1,4-dioxane (50 ml) and 4N hydrogen chloride/1,4-dioxane solution (250 ml), and the mixture was stirred under room temperature for 2 hours. The solvent was removed under a reduced pressure and toluene was added and reevaporated to give L-phenylalanine 4-carbamoylanilide hydrochloride (II) quantitatively as a white powder. On the other hand, trans-4-(t-butoxycarbonylaminomethyl)cyclohexylcarboxylic acid (13.36 g) was dissolved in dry tetrahydrofuran (500 ml), and triethylamine (7.80 ml) was added under ice-cooling, followed by stirring at the same temperature for 10 minutes. Subsequently, a solution of ethyl chlorocarbonate (5.64 g) in dry tetrahydrofuran (50 ml) was added dropwise under ice-cooling for 3 minutes, and the mixture was again stirred at the same temperature for 20 minutes. The above mixture was added to the suspension of the hydrochloride (II) previously obtained and triethylamine (8.53 ml) in N,N-dimethylformamide (150 ml) under ice-cooling, followed by stirring at the same temperature for 2 hours, and under room temperature for 6 hours. Ice-water (1.4 liter) was added and the insolubles were collected by filtration, thoroughly washed with water, and further washed with 10% aqueous citric acid, water 5% aqueous sodium hydrogen carbonate, followed by washing with water at 40° to 50° C., and drying, to give N-[4-trans-(t-butoxycarbonylaminomethyl)cyclohexylcarbonyl]-L-phenylalanine 4-carbamoylanilide (III) (24.63 g). The structure was confirmed by NMR.

後処理

  1. temperaturecooling
  2. temperaturecooling for 3 minutes
  3. stirringthe mixture was again stirred at the same temperature for 20 minutes
  4. custompreviously obtained
  5. stirringby stirring at the same temperature for 2 hours
  6. waitunder room temperature for 6 hours
  7. filtrationthe insolubles were collected by filtration
  8. washthoroughly washed with water
  9. washfurther washed with 10% aqueous citric acid, water 5% aqueous sodium hydrogen carbonate
  10. washby washing with water at 40° to 50° C.
  11. customdrying

出典と根拠

ORDレコード
ord-a755bcc8a388454da3f63393f55da0be
出典データセット
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04954512

反応ノート

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