3-(Chloromethyl)pyridine → HCID 20228664, compound

HRID 1731365Notes

Reaction equation

HRID 1731365 reaction equation
[CH3:1][C:2]1[N:6]2[CH:7]=[CH:8][C:9]([CH3:11])=[CH:10][C:5]2=[N:4][C:3]=1[C:12]1[CH:13]=[CH:14][C:15]2[S:19][C:18](=[O:20])[NH:17][C:16]=2[CH:21]=1.Cl[CH2:23][C:24]1[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=1>>[CH3:1][C:2]1[N:6]2[CH:7]=[CH:8][C:9]([CH3:11])=[CH:10][C:5]2=[N:4][C:3]=1[C:12]1[CH:13]=[CH:14][C:15]2[S:19][C:18](=[O:20])[N:17]([CH2:23][C:24]3[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=3)[C:16]=2[CH:21]=1

Participants

3

Reactant 2

HCID 183583-(Chloromethyl)pyridineHCID 202287175-(3,7-Dimethylimidazo[1,2-a]pyridin-2-yl)-1,3-benzothiazol-2(3H)-one

Product 1

HCID 20228664HCID 20228664, compoundYield 47.5%

Procedure

5-(3,7-Dimethylimidazo[1,2-a]pyridin-2-yl)-3-(pyridin-3-ylmethyl)-2-benzothiazolinone (0.92 g) was prepared in substantially the same manner as that of Example 47 from 5-(3,7-dimethylimidazo[1,2-a]pyridin-2-yl)-2-benzothiazolinone (1.48 g) and 3-chloromethylpyridine (1.27 g). mp. 201°-202° C.

Sources & evidence

ORD record
ord-ef9e984c773444c2bc1b99fd19c6424a
Source dataset
uspto-grants-1986_11
Patent number
US04621084

Reaction notes

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