Dicyclohexylcarbodiimide → HCID 14182508, Verbindung

HRID 1252621

Reaktionsgleichung

Reaktionsgleichung von HRID 1252621
[C:1]1([CH2:7][O:8][C:9]2[C:14]([O:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:13][N:12]=[C:11]([C:23]([OH:25])=O)[CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.OC1C2N=NNC=2C=CC=1.[NH2:36][N:37]1[CH2:42][CH2:41][NH:40][C:39](=[O:43])[C:38]1=[O:44].C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C=O>[O:44]=[C:38]1[C:39](=[O:43])[NH:40][CH2:41][CH2:42][N:37]1[NH:36][C:23]([C:11]1[CH:10]=[C:9]([O:8][CH2:7][C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:14]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:13][N:12]=1)=[O:25]

Komponenten

6

Versuchsvorschrift

To a suspension of 4,5-bis(phenylmethoxy)-2-pyridinecarboxylic acid (7.1 g, 21.17 mmol), hydroxybenzotriazole (0.29 g, 2.12 mmol) and N-aminopiperazine-2,3-dione (2.73 g, 21.17 mmol) in 140 ml of dry dimethylformamide was added, after 15 minutes of stirring, 4.80 g (23.3 mmol) of dicyclohexylcarbodiimide. After stirring for 21 hours at room temperature, dicyclohexylurea was filtered off (4.0 g ) and the solvent was evaporated in vacuo. The solid residue was triturated for 40 minutes with 240 ml of tetrahydrofuran, filtered, washed with tetrahyrofuran and dried in vacuo to yield 7.76 g of the title compound, melting point 231.1° C.

Aufarbeitung

  1. additionwas added, after 15 minutes
  2. stirringAfter stirring for 21 hours at room temperature
  3. filtrationdicyclohexylurea was filtered off (4.0 g )
  4. customthe solvent was evaporated in vacuo
  5. customThe solid residue was triturated for 40 minutes with 240 ml of tetrahydrofuran
  6. filtrationfiltered
  7. washwashed with tetrahyrofuran
  8. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-81ed4b1db5334fe3bea74590afbf00bf
Quelldatensatz
uspto-grants-1988_05
Patentnummer
US04743685

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