HCID 14198890, compound → HCID 58530480, compound

HRID 2400892Notes

Reaction equation

HRID 2400892 reaction equation
[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([CH2:6][N:7]2[C:11]3[CH:12]=[CH:13][C:14]([CH:16]=O)=[CH:15][C:10]=3[N:9]=[N:8]2)=[C:4]([C:20]([F:23])([F:22])[F:21])[CH:3]=1.O1CCCCC1[O:30][N:31]1[C:35](=[O:36])[CH2:34][S:33][C:32]1=[O:37]>>[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([CH2:6][N:7]2[C:11]3[CH:12]=[CH:13][C:14](/[CH:16]=[C:34]4/[C:35](=[O:36])[N:31]([OH:30])[C:32](=[O:37])[S:33]/4)=[CH:15][C:10]=3[N:9]=[N:8]2)=[C:4]([C:20]([F:23])([F:21])[F:22])[CH:3]=1

Participants

3

Reactant 2

HCID 14198890HCID 14198890, compoundHCID 86659634HCID 86659634, compound

Product 1

HCID 58530480HCID 58530480, compound

Procedure

(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-1H-benzotriazol-5-yl}methylidene)-3-hydroxy-1,3-thiazolidine-2,4-dione was prepared from 1-(4-chloro-2-trifluoromethylbenzyl)-1H-benzotriazole-5-carbaldehyde (from Example 258) and 3-(tetrahydropyran-2-yl)oxy-1,3-thiazolidine-2,4-dione (from Example 288) following General Procedure F.

Sources & evidence

ORD record
ord-3792d0b6f7574361a470accb51b688a1
Source dataset
uspto-grants-2014_08
Patent number
US08796256B2

Reaction notes

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