(2,4-Dioxo-1,3-thiazolidin-3-yl)acetic acid → HCID 58530686, compound

HRID 2401009

Reaction equation

HRID 2401009 reaction equation
[Cl:1][C:2]1[CH:26]=[CH:25][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12]([CH:16]=O)=[CH:13][CH:14]=3)[C:9]([C:18]3[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=3)=[N:8]2)=[C:4]([C:27]([F:30])([F:29])[F:28])[CH:3]=1.[O:31]=[C:32]1[N:36]([CH2:37][C:38]([OH:40])=[O:39])[C:35](=[O:41])[CH2:34][S:33]1>>[Cl:1][C:2]1[CH:26]=[CH:25][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12](/[CH:16]=[C:34]4/[C:35](=[O:41])[N:36]([CH2:37][C:38]([OH:40])=[O:39])[C:32](=[O:31])[S:33]/4)=[CH:13][CH:14]=3)[C:9]([C:18]3[CH:19]=[CH:20][C:21]([F:24])=[CH:22][CH:23]=3)=[N:8]2)=[C:4]([C:27]([F:29])([F:30])[F:28])[CH:3]=1

Participants

3

Reactant 2

HCID 2770836(2,4-Dioxo-1,3-thiazolidin-3-yl)acetic acidHCID 86659710HCID 86659710, compound

Product 1

HCID 58530686HCID 58530686, compound

Procedure

[(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-3-(4-fluorophenyl)-1H-indazol-5-yl}methylidene)-2,4-dioxo-1,3-thiazolidin-3-yl]acetic acid was prepared from 1-(4-chloro-2-trifluoromethylbenzyl)-3-(4-fluorophenyl)-1H-indazole-5-carbaldehyde and (2,4-dioxothiazolidin-3-yl)acetic acid following General Procedure F.

Sources & evidence

ORD record
ord-715284b356914ce3b5747d6e7de83fde
Source dataset
uspto-grants-2014_08
Patent number
US08796256B2

Linked notes

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