4-[9-(2,2,2-Trifluoroethylcarbamoyl)-9H-xanthen-9-yl]butyl bromide → HCID 23526838, compound

HRID 2415990Notes

Reaction equation

HRID 2415990 reaction equation
[F:1][C:2]([F:27])([F:26])[CH2:3][NH:4][C:5]([C:7]1([CH2:21][CH2:22][CH2:23][CH2:24]Br)[C:20]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[O:14][C:13]2[C:8]1=[CH:9][CH:10]=[CH:11][CH:12]=2)=[O:6].[CH3:28][C@H:29]1[NH:34][C@@H:33]([CH3:35])[CH2:32][N:31]([C:36]2[S:37][C:38]3[CH:44]=[CH:43][CH:42]=[CH:41][C:39]=3[N:40]=2)[CH2:30]1>>[F:1][C:2]([F:27])([F:26])[CH2:3][NH:4][C:5]([C:7]1([CH2:21][CH2:22][CH2:23][CH2:24][N:34]2[C@H:33]([CH3:35])[CH2:32][N:31]([C:36]3[S:37][C:38]4[CH:44]=[CH:43][CH:42]=[CH:41][C:39]=4[N:40]=3)[CH2:30][C@@H:29]2[CH3:28])[C:20]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[O:14][C:13]2[C:8]1=[CH:9][CH:10]=[CH:11][CH:12]=2)=[O:6]

Participants

3

Reactant 2

HCID 221802034-[9-(2,2,2-Trifluoroethylcarbamoyl)-9H-xanthen-9-yl]butyl bromideHCID 69891670HCID 69891670, compound

Product 1

HCID 23526838HCID 23526838, compound

Procedure

Prepared analogously to Example 1 from 9-(4-bromo-butyl)-9H-xanthene-9-carboxylic acid-(2,2,2-trifluoro-ethyl)-amide and 2-(cis-3,5-dimethyl-piperazin-1-yl)-benzothiazole.

Sources & evidence

ORD record
ord-e4a671f39bb642bd877d79ffe74da0ea
Source dataset
uspto-grants-2004_11
Patent number
US06821967B2

Reaction notes

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