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

HRID 1750043Notes

Reaction equation

HRID 1750043 reaction equation
Cl[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH3:12])[C:5]=2[N:6]=1.FC(F)(F)C(O)=O.[NH:20]1[CH2:24][CH2:23][CH:22]([CH2:25][O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[NH:33][S:34]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][N:38]=2)(=[O:36])=[O:35])[CH2:21]1>>[CH3:12][O:11][C:7]1[C:5]2[N:6]=[C:2]([N:20]3[CH2:24][CH2:23][CH:22]([CH2:25][O:26][C:27]4[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=4[NH:33][S:34]([C:37]4[CH:42]=[CH:41][CH:40]=[CH:39][N:38]=4)(=[O:35])=[O:36])[CH2:21]3)[S:3][C:4]=2[CH:10]=[CH:9][CH:8]=1

Participants

3

Reactant 2

HCID 20498622-Chloro-4-methoxy-1,3-benzothiazoleHCID 67609894N-(2-(pyrrolidin-3-ylmethoxy)phenyl)pyridine-2-sulfonamide trifluoroacetate

Product 1

HCID 67607737N-(2-((1-(4-methoxybenzo[d]thiazol-2-yl)pyrrolidin-3-yl)methoxy)-phenyl)pyridine-2-sulfonamide

Procedure

Compound 32 is prepared using synthesis method 3 using intermediates 2c and 6b (yield: 51%).

Sources & evidence

ORD record
ord-0b7d2913883b423786868da3d79e1d79
Source dataset
uspto-grants-2015_10
Patent number
US09156834B2

Reaction notes

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