Di-p-tolylcarbodiimide → HCID 178426524, Verbindung

HRID 1813887Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1813887
Cl.[CH2:2]([O:9][C:10](=[O:23])[C@H:11]([CH2:13][C:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[NH:16][CH:15]=1)N)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C([N:27](C(C)C)CC)(C)C.[C:33]1([CH3:49])[CH:38]=[CH:37][C:36]([N:39]=[C:40]=[N:41][C:42]2[CH:47]=[CH:46][C:45]([CH3:48])=[CH:44][CH:43]=2)=[CH:35][CH:34]=1>CN(C=O)C>[C:33]1([CH3:49])[CH:38]=[CH:37][C:36]([N:39]([CH:11]([CH2:13][C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[NH:16][CH:15]=2)[C:10]([O:9][CH2:2][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=2)=[O:23])[C:40]([NH:41][C:42]2[CH:43]=[CH:44][C:45]([CH3:48])=[CH:46][CH:47]=2)=[NH:27])=[CH:35][CH:34]=1

Komponenten

5

Versuchsvorschrift

1.0 mmol of tryptophan benzyl ester hydrochloride was dissolved in 20 ml of DMF and 1.1 mmol of diisopropylethylamine was added. After 10 min, 1.0 mmol of 1,3 di-p-tolylcarbodiimide was added to the stirred solution. The reaction mixture was stirred overnight in room temperature. The precipitated solid was filtered off and washed twice with 1 ml of DMF. To the collected filtrate, 50 ml of water was added. The precipitated solid was collected by filtration and washed with water. The solid was dissolved in ethyl acetate and 0.1 ml of conc. HCl was added. The pure product was precipitated from the solution with ethyl ether. Yield of pure compound=79%.

Aufarbeitung

  1. filtrationThe precipitated solid was filtered off
  2. washwashed twice with 1 ml of DMF
  3. additionTo the collected filtrate, 50 ml of water was added
  4. filtrationThe precipitated solid was collected by filtration
  5. washwashed with water
  6. dissolutionThe solid was dissolved in ethyl acetate
  7. addition0.1 ml of conc. HCl was added
  8. customThe pure product was precipitated from the solution with ethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-f3d466c8f3b941adb6358af8846a5256
Quelldatensatz
uspto-grants-2005_04
Patentnummer
US06875759B1

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