Hydrochloric Acid → 1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochloride
Reaktionsgleichung
C[O:2][C:3](=[O:21])[CH2:4][C:5]1[N:9]([CH2:10][C:11]2[CH:20]=[CH:19][C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH:12]=2)[CH:8]=[N:7][CH:6]=1.[ClH:22]>>[ClH:22].[CH:12]1[C:13]2[C:18](=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:19]=[CH:20][C:11]=1[CH2:10][N:9]1[C:5]([CH2:4][C:3]([OH:21])=[O:2])=[CH:6][N:7]=[CH:8]1Komponenten
3
Reaktionsbedingungen
- Temperatur
- 55 °C
Versuchsvorschrift
2-[1-(Naphth-2-ylmethyl)-1H-imidazol-5-yl]acetic acid methyl ester (0.92 g, 3.28 mmol ) was dissolved in 2.5N hydrochloric acid (50 ml ) and heated to 55° C. for 3 hr. After this time, the solution was concentrated to dryness in vacuo to give the title compound as a white solid.
Aufarbeitung
- concentrationAfter this time, the solution was concentrated to dryness in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-88c59fffcc834ac3b37a55225513e4e1
- Quelldatensatz
- uspto-grants-1999_04
- Patentnummer
- US05891889
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