Cyclohexane → HCID 70085481, compound
Reaction equation
[SH:1][C:2]1[S:6][C:5]([S:7][CH2:8][N:9]2[C:19](=[O:20])[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[S:10]2(=[O:12])=[O:11])=[N:4][N:3]=1.Cl.Cl[CH2:23][CH2:24][N:25]([CH2:28][CH3:29])[CH2:26][CH3:27].C(N(CC)CC)C.C1CCCCC1>CN(C=O)C.C(OCC)(=O)C>[CH2:24]([N:25]([CH2:28][CH3:29])[CH2:26][CH2:27][S:1][C:2]1[S:6][C:5]([S:7][CH2:8][N:9]2[C:19](=[O:20])[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[S:10]2(=[O:12])=[O:11])=[N:4][N:3]=1)[CH3:23]Participants
7
Procedure
Following a procedure similar to that described in Example 33A, 2-(5-mercapto-1,3,4-thiadiazol-2-ylthiomethyl)saccharin is reacted with 2-chloroethyldiethylamine hydrochloride in DMF in the presence of triethylamine to give 2-(5-[2-(diethylamino)ethylthio]-1,3,4-thiadiazol-2-ylthiomethyl)saccharin, mp 93.0°-94.5° C. (from cyclohexane:ethyl acetate).
Sources & evidence
- ORD record
- ord-bcac902a6a644a2d9333eeccf811f580
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05650422
Reaction notes
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