(5-Methoxymethyl-pyrrolidin-3-yl)-methyl-amine → 5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-1H-indazol-5-ylmethylene]-2-[(5-methoxymethyl-pyrrolidin-3-yl)-methyl-amino]-thiazol-4-one

HRID 1970159Notes

Reaction equation

HRID 1970159 reaction equation
[Cl:1][C:2]1[CH:27]=[CH:26][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12]([CH:16]=[C:17]4[S:21][CH:20](SCC)[NH:19][C:18]4=[O:25])=[CH:13][CH:14]=3)[CH:9]=[N:8]2)=[C:4]([C:28]([F:31])([F:30])[F:29])[CH:3]=1.[CH3:32][O:33][CH2:34][CH:35]1[NH:39][CH2:38][CH:37]([NH:40][CH3:41])[CH2:36]1>>[Cl:1][C:2]1[CH:27]=[CH:26][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][C:12]([CH:16]=[C:17]4[S:21][C:20]([N:40]([CH:37]5[CH2:36][CH:35]([CH2:34][O:33][CH3:32])[NH:39][CH2:38]5)[CH3:41])=[N:19][C:18]4=[O:25])=[CH:13][CH:14]=3)[CH:9]=[N:8]2)=[C:4]([C:28]([F:31])([F:30])[F:29])[CH:3]=1

Participants

3

Procedure

5-[1-(4-Chloro-2-trifluoromethyl-benzyl)-1H-indazol-5-ylmethylene]-2-[(5-methoxymethyl-pyrrolidin-3-yl)-methyl-amino]-thiazol-4-one was prepared from 5-[1-(4-chloro-2-trifluoromethyl-benzyl)-1H-indazol-5-ylmethylene]-2-ethylsulfanyl-thiazolidin-4-one and (5-Methoxymethyl-pyrrolidin-3-yl)-methyl-amine following General Procedure C.

Sources & evidence

ORD record
ord-074da5e5f42e46c7be531efd137f5814
Source dataset
uspto-grants-2013_04
Patent number
US08426604B2

Reaction notes

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