4-Methylmorpholine → HCID 178474779, Verbindung

HRID 1106116Notizen

Reaktionsgleichung

[C:1]([NH:4][C@H:5]([C:11]([OH:13])=O)[CH2:6][CH2:7][C:8](=[O:10])[NH2:9])(=[O:3])[CH3:2].C(N(CC)CC)C.C(OC(Cl)=O)C(C)C.[NH2:29][C:30]1[CH:35]=[CH:34][C:33]([C:36]2[N:41]=[C:40]([OH:42])[C:39]([C:43]([OH:45])=[O:44])=[CH:38][N:37]=2)=[CH:32][CH:31]=1.CN1CCOCC1>CN(C)C=O>[C:1]([NH:4][CH:5]([C:11]([NH:29][C:30]1[CH:31]=[CH:32][C:33]([C:36]2[N:41]=[C:40]([OH:42])[C:39]([C:43]([OH:45])=[O:44])=[CH:38][N:37]=2)=[CH:34][CH:35]=1)=[O:13])[CH2:6][CH2:7][C:8](=[O:10])[NH2:9])(=[O:3])[CH3:2]

Komponenten

Reaktionsbedingungen

Temperatur: 5 °C

Versuchsvorschrift

A solution of 14.1 g (75 mmol) of N-acetyl-L-glutamine and 9.75 ml (75 mmol) of triethylamine in 150 ml of dimethylformamide is stirred at -15° to -20° C. and 9.75 ml (75 mmol) of isobutylchloroformate is added. After stirring at -15° to -20° C. for 30 min a cold solution of 11.6 g (50 mmol) of 2-(4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid and 7.15 ml (50 mml) of N-methylmorpholine in 200 ml of dimethylformamide is added at -15° C. The reaction mixture is stirred at -15° for 20 min at 5° C. for 3 hrs, and at room temperature overnight. The reaction mixture is evaporated and the residue treated with water. The pH is lowered to 2.5 with hydrochloric acid and the solid is filtered, washed with water, and dried to afford 17.3 g of 2-[4-(N-acetyl-DL-glutaminylamino)phenyl]4-hydroxy-5-pyrimidine carboxylic acid; mp 247°-248° C. dec. [α]23D -2.8° (c0.7, DMSO)

Aufarbeitung

additionis added at -15° C
customat room temperature
customovernight
customThe reaction mixture is evaporated
additionthe residue treated with water
filtrationthe solid is filtered
washwashed with water
customdried

Quellen und Nachweise

ORD-Eintrag: ord-3582722e0c73412ca77c0a1d2352e0ac
Quelldatensatz: uspto-grants-1982_01
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US04311699

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