5-(Toluene-4-sulfonyl)-thiazolidine-2,4-dione → 5-Pent-4-ynyl-5-(toluene-4-sulfonyl)-thiazolidine-2,4-dione
Reaction equation
I[CH2:2][CH2:3][CH2:4][C:5]#[CH:6].[C:7]1([CH3:23])[CH:12]=[CH:11][C:10]([S:13]([CH:16]2[S:20][C:19](=[O:21])[NH:18][C:17]2=[O:22])(=[O:15])=[O:14])=[CH:9][CH:8]=1>>[CH2:2]([C:16]1([S:13]([C:10]2[CH:11]=[CH:12][C:7]([CH3:23])=[CH:8][CH:9]=2)(=[O:14])=[O:15])[S:20][C:19](=[O:21])[NH:18][C:17]1=[O:22])[CH2:3][CH2:4][C:5]#[CH:6]Participants
3
Procedure
In the manner of Example 100 above, 5-iodo-1-pentyne is created with 5-(toluene-4-sulfonyl)-thiazolidine-2,4-dione to give the title compound, mp 226° C., THEORY: C,53.4, H, 4.48, N, 4.15 FOUND: C, 53.3, H, 4.58, N, 4.13.
Sources & evidence
- ORD record
- ord-1af79ca61ba040faad820c17a13c14f2
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06784184B2
Reaction notes
Loading…