2-Chloro-4-methylbenzothiazole → N-(2-((1-(4-methylbenzo[d]thiazol-2-yl)pyrrolidin-3-yl)methoxy)phenyl)pyridine-2-sulfonamide

HRID 84173

Reaction equation

HRID 84173 reaction equation
Cl[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:5]=2[N:6]=1.FC(F)(F)C(O)=O.[NH:19]1[CH2:23][CH2:22][CH:21]([CH2:24][O:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[NH:32][S:33]([C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=2)(=[O:35])=[O:34])[CH2:20]1>>[CH3:11][C:7]1[C:5]2[N:6]=[C:2]([N:19]3[CH2:23][CH2:22][CH:21]([CH2:24][O:25][C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=4[NH:32][S:33]([C:36]4[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=4)(=[O:34])=[O:35])[CH2:20]3)[S:3][C:4]=2[CH:10]=[CH:9][CH:8]=1

Participants

3

Reactant 2

HCID 20498602-Chloro-4-methylbenzothiazoleHCID 67609894N-(2-(pyrrolidin-3-ylmethoxy)phenyl)pyridine-2-sulfonamide trifluoroacetate

Product 1

HCID 67608714N-(2-((1-(4-methylbenzo[d]thiazol-2-yl)pyrrolidin-3-yl)methoxy)phenyl)pyridine-2-sulfonamide

Procedure

Compound 31 is prepared using synthesis method 3 using intermediates 2b and 6b (yield: 28%).

Sources & evidence

ORD record
ord-b3a70ef77559445e94eed95630cff817
Source dataset
uspto-grants-2014_09
Patent number
US08846930B2

Linked notes

Loading…