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Thiazolidinedione → 5-(3'-Methylaminobiphenyl-4-ylmethylene)thiazolidine-2,4-dione

HRID 1072114
Notes
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Reaction equation

HRID 1072114 reaction equation
[CH3:1][NH:2][C:3]1[CH:4]=[C:5]([C:9]2[CH:14]=[CH:13][C:12]([CH:15]=O)=[CH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1.[S:17]1[CH2:21][C:20](=[O:22])[NH:19][C:18]1=[O:23]>>[CH3:1][NH:2][C:3]1[CH:4]=[C:5]([C:9]2[CH:10]=[CH:11][C:12]([CH:15]=[C:21]3[S:17][C:18](=[O:23])[NH:19][C:20]3=[O:22])=[CH:13][CH:14]=2)[CH:6]=[CH:7][CH:8]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 5437ThiazolidinedioneHCID 13945243'-Methylaminobiphenyl-4-carbaldehyde

Product 1

HCID 865989415-(3'-Methylaminobiphenyl-4-ylmethylene)thiazolidine-2,4-dioneYield 91.7%

Procedure

In a manner similar to Example 1(d), by reacting 2.9 g (13.7 mmol) of 3′-methylaminobiphenyl-4-carbaldehyde with 1.6 g (13.7 mmol) of 2,4-thiazolidinedione, 3.9 g (91%) of the expected product are obtained after trituration in dichloromethane and ether.

Sources & evidence

ORD record
ord-0aa5c15601254fd2951ec3507b577b1f
Source dataset
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
On this pageParticipantsProcedureSources & evidenceReaction notes
Patent number
US06908939B2

Reaction notes

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