Thiazolidinedione → HCID 54113008, compound

HRID 257191Notes

Reaction equation

HRID 257191 reaction equation
[CH3:1][N:2]([CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:23]=[CH:22][C:19]([CH:20]=O)=[CH:18][CH:17]=1)[C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1.[S:24]1[CH2:28][C:27](=[O:29])[NH:26][C:25]1=[O:30]>>[CH3:1][N:2]([CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:23]=[CH:22][C:19]([CH:20]=[C:28]2[S:24][C:25](=[O:30])[NH:26][C:27]2=[O:29])=[CH:18][CH:17]=1)[C:3]1[O:4][C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[N:7]=1

Participants

3

Reactant 2

HCID 5437ThiazolidinedioneHCID 10267393HCID 10267393, compound

Product 1

HCID 54113008HCID 54113008, compound

Procedure

The title compound (m.p. 202°-204° C.) was prepared from 4-[3-(N-methyl-N-(2-benzoxazolyl)amino)propoxy]benzaldehyde (5.3 g) and 2,4-thiazolidinedione (2,2 g) by a similar procedure to that described in Example 4,

Sources & evidence

ORD record
ord-77a9d50d3d5545ec86c03644e671526c
Source dataset
uspto-grants-1993_11
Patent number
US05260445

Reaction notes

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