Ethyl 4-amino-phenyloxyacetate hydrochloride → HCID 178473010, Verbindung
Reaktionsgleichung
[NH:1]([C:5]1[S:6][CH:7]=[C:8]([C:10]([OH:12])=O)[N:9]=1)[C:2]([NH2:4])=[NH:3].Cl.[NH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:17][CH:16]=1>>[NH:1]([C:5]1[S:6][CH:7]=[C:8]([C:10]([NH:14][C:15]2[CH:16]=[CH:17][C:18]([O:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])=[CH:19][CH:20]=2)=[O:12])[N:9]=1)[C:2]([NH2:4])=[NH:3]Komponenten
3
Versuchsvorschrift
In the same manner as described in Example 3, from 2-guanidino-thiazole-4-carboxylic acid and ethyl 4-amino-phenyloxyacetate hydrochloride there is obtained ethyl {4-[(2-guanidino-thiazole-4-carbonyl)-amino]-phenoxy}-acetate, m.p. 206° C., MS: 364 (M+H)+.
Quellen und Nachweise
- ORD-Eintrag
- ord-ad020ac68e7148c48a9d2bae5319fc7e
- Quelldatensatz
- uspto-grants-2001_10
- Patentnummer