Thiazolidinedione → HCID 53954799, compound

HRID 2253653Notes

Reaction equation

HRID 2253653 reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[NH:10][CH2:11][CH2:12][O:13][C:14]1[CH:21]=[CH:20][C:17]([CH:18]=O)=[CH:16][CH:15]=1.[S:22]1[CH2:26][C:25](=[O:27])[NH:24][C:23]1=[O:28]>>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[NH:10][CH2:11][CH2:12][O:13][C:14]1[CH:21]=[CH:20][C:17]([CH:18]=[C:26]2[S:22][C:23](=[O:28])[NH:24][C:25]2=[O:27])=[CH:16][CH:15]=1

Participants

3

Reactant 2

HCID 5437ThiazolidinedioneHCID 10423882HCID 10423882, compound

Product 1

HCID 53954799HCID 53954799, compound

Procedure

The title compound (m.p. 242°-5° C.) was prepared from 4-[2-(N-(2-benzoxazolyl)amino)ethoxy]benzaldehyde (5.18 g) and 2,4-thiazolidinedione (2.36 g) by a similar procedure to that described in Example 4.

Sources & evidence

ORD record
ord-4e189c3c766a4e91b8a94e8478fb0c3d
Source dataset
uspto-grants-1993_08
Patent number
US05232925

Reaction notes

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