2-Piperidino-4-imino-2-thiazoline hydrochloride → HCID 178436757, Verbindung
Reaktionsgleichung
[CH3:1][O:2][C:3]1[C:11]([O:12][CH3:13])=[CH:10][C:9]([O:14][CH3:15])=[C:8]2[C:4]=1[C:5](=N)[NH:6][C:7]2=[NH:16].[ClH:18].[CH2:19]([CH:21]1[CH2:25][CH2:24][N:23]([C:26]2[S:27][CH2:28][C:29](=[NH:31])[N:30]=2)[CH2:22]1)[CH3:20].N=C1C2C(=CC=CC=2)C(=N)N1.Cl.N1(C2SCC(=N)N=2)CCCCC1>>[ClH:18].[NH:16]=[C:7]1[C:8]2[C:4](=[C:3]([O:2][CH3:1])[C:11]([O:12][CH3:13])=[CH:10][C:9]=2[O:14][CH3:15])[C:5](=[C:28]2[S:27][C:26]([N:23]3[CH2:24][CH2:25][CH:21]([CH2:19][CH3:20])[CH2:22]3)=[N:30][C:29]2=[NH:31])[NH:6]1Komponenten
5
Versuchsvorschrift
When equivalent amounts of 4,5,7-trimethoxy-1,3-diiminoisoindoline and 2-(3-ethylpyrrolidino)-4-imino-2-thiazoline hydrochloride are substituted for the 1,3-diiminoisoindoline and 2-piperidino-4-imino-2-thiazoline hydrochloride respectively, in the procedure described in Example 9, part C above, there is obtained as the product 1-imino-4,5,7-trimethoxy-3-[2-(3-ethylpyrrolidino)-4-imino-2-thiazolin-5-ylidene]isoindoline hydrochloride.
Quellen und Nachweise
- ORD-Eintrag
- ord-9f2296c006d24b9e85ccc75951b6d862
- Quelldatensatz
- uspto-grants-1978_10
- Patentnummer
- US04122261
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