1-Pyrrolidineethanol → (5Z)-5-({3-Chloro-1-[4-chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}-methylidene)-3-(2-pyrrolidin-1-ylethyl)-1,3-thiazolidine-2,4-dione

HRID 2400902Notes

Reaction equation

HRID 2400902 reaction equation
[Cl:1][C:2]1[CH:30]=[CH:29][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12](/[CH:16]=[C:17]4/[C:18](=[O:27])[N:19]([CH2:23][C:24](O)=O)[C:20](=[O:22])[S:21]/4)=[CH:13][CH:14]=3)[C:9]([Cl:28])=[N:8]2)=[C:4]([C:31]([F:34])([F:33])[F:32])[CH:3]=1.OCC[N:38]1[CH2:42][CH2:41][CH2:40][CH2:39]1>>[Cl:28][C:9]1[C:10]2[C:15](=[CH:14][CH:13]=[C:12](/[CH:16]=[C:17]3/[C:18](=[O:27])[N:19]([CH2:23][CH2:24][N:38]4[CH2:42][CH2:41][CH2:40][CH2:39]4)[C:20](=[O:22])[S:21]/3)[CH:11]=2)[N:7]([CH2:6][C:5]2[CH:29]=[CH:30][C:2]([Cl:1])=[CH:3][C:4]=2[C:31]([F:34])([F:32])[F:33])[N:8]=1

Participants

3

Procedure

(5Z)-5-({3-Chloro-1-[4-chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}-methylidene)-3-(2-pyrrolidin-1-ylethyl)-1,3-thiazolidine-2,4-dione was prepared from [(5Z)-5-({3-chloro-1-[4-chloro-2-(trifluoromethyl)benzyl]-1H-indazol-5-yl}methylidene)-2,4-dioxo-1,3-thiazolidine (from Example 287) and 1-(2-hydroxyethyl)pyrrolidine following General Procedure J.

Sources & evidence

ORD record
ord-47687233ac7a4d0b910b1abaa7d528b6
Source dataset
uspto-grants-2014_08
Patent number
US08796256B2

Reaction notes

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