173019-82-4 → 5-(Benzoxazol-2-ylsulfanyl)-5-[3-(4-chlorophenyl)-prop-2-ynyl]-thiazolidine-2,4-dione
Reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[S:10][CH:11]1[S:15][C:14](=[O:16])[NH:13][C:12]1=[O:17].[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([C:25]#[C:26][CH2:27]Br)=[CH:21][CH:20]=1.FC1C=C(C#CCBr)C=C(F)C=1>>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[S:10][C:11]1([CH2:27][C:26]#[C:25][C:22]2[CH:23]=[CH:24][C:19]([Cl:18])=[CH:20][CH:21]=2)[S:15][C:14](=[O:16])[NH:13][C:12]1=[O:17]Participants
4
Procedure
Prepared from 5-(benzoxazol-2-ylsulfanyl)-thiazolidine-2,4-dione, (III), Example 89 and [3-(4-chlorophenyl)-prop-2-ynyl]-bromide of formula (IX), Example mp 137°-139° C.; Anal. Calc. for C19H11ClN2O3S2 : C, 55.80; H, 2.67; N, 6.75; Found: C, 54.92; H, 2.76; N, 6.82.
Sources & evidence
- ORD record
- ord-f4ae3802ce6d49fdae4280cdb5de7d38
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05574051
Reaction notes
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