2-Chloro-6-methoxybenzothiazole → HCID 59643376, compound

HRID 2251556Notes

Reaction equation

HRID 2251556 reaction equation
[CH3:1][C:2]([O:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][NH:18][CH2:19][C:20]2[CH:25]=[CH:24][C:23]([C:26]([F:29])([F:28])[F:27])=[CH:22][CH:21]=2)=[CH:12][CH:11]=1)([CH3:8])[C:3]([O:5]CC)=[O:4].Cl[C:31]1[S:32][C:33]2[CH:39]=[C:38]([O:40][CH3:41])[CH:37]=[CH:36][C:34]=2[N:35]=1>>[CH3:41][O:40][C:38]1[CH:37]=[CH:36][C:34]2[N:35]=[C:31]([N:18]([CH2:19][C:20]3[CH:21]=[CH:22][C:23]([C:26]([F:28])([F:27])[F:29])=[CH:24][CH:25]=3)[CH2:17][CH2:16][C:13]3[CH:14]=[CH:15][C:10]([O:9][C:2]([CH3:1])([CH3:8])[C:3]([OH:5])=[O:4])=[CH:11][CH:12]=3)[S:32][C:33]=2[CH:39]=1

Participants

3

Reactant 2

HCID 2731322-Chloro-6-methoxybenzothiazoleHCID 59643115HCID 59643115, compound

Product 1

HCID 59643376HCID 59643376, compound

Procedure

Similarly prepared from ethyl 2-methyl-2-[4-(2-{[4-(trifluoromethyl)benzyl]amino}ethyl)phenoxy]propanoate and 2-chloro-6-methoxy benzothiazole.

Sources & evidence

ORD record
ord-dfcf0b4bf7564a21aadf724a001fb19d
Source dataset
uspto-grants-2008_01
Patent number
US07319104B2

Reaction notes

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