2,6-Dichlorobenzothiazole → HCID 59643261, compound

HRID 2251558Notes

Reaction equation

HRID 2251558 reaction equation
[F:1][C:2]([F:32])([F:31])[C:3]1[CH:26]=[C:25]([C:27]([F:30])([F:29])[F:28])[CH:24]=[CH:23][C:4]=1[CH2:5][NH:6][CH2:7][CH2:8][C:9]1[CH:22]=[CH:21][C:12]([O:13][C:14]([CH3:20])([CH3:19])[C:15]([O:17]C)=[O:16])=[CH:11][CH:10]=1.Cl[C:34]1[S:35][C:36]2[CH:42]=[C:41]([Cl:43])[CH:40]=[CH:39][C:37]=2[N:38]=1>>[F:1][C:2]([F:31])([F:32])[C:3]1[CH:26]=[C:25]([C:27]([F:30])([F:29])[F:28])[CH:24]=[CH:23][C:4]=1[CH2:5][N:6]([C:34]1[S:35][C:36]2[CH:42]=[C:41]([Cl:43])[CH:40]=[CH:39][C:37]=2[N:38]=1)[CH2:7][CH2:8][C:9]1[CH:22]=[CH:21][C:12]([O:13][C:14]([CH3:20])([CH3:19])[C:15]([OH:17])=[O:16])=[CH:11][CH:10]=1

Participants

3

Reactant 2

HCID 771762,6-DichlorobenzothiazoleHCID 59643248HCID 59643248, compound

Product 1

HCID 59643261HCID 59643261, compound

Procedure

Similarly prepared from methyl 2-[4-(2-{[2,4-bis(trifluoromethyl)benzyl]amino}ethyl)phenoxy]-2-methylpropanoate and 2,6-dichloro benzothiazole.

Sources & evidence

ORD record
ord-e3f60c9c7a284dbba531b1f0e25ccb6f
Source dataset
uspto-grants-2008_01
Patent number
US07319104B2

Reaction notes

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