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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748482Generated: October 29, 2026

4-(Chloromethyl)-2-methyl-1,3-thiazole → HCID 59750622, compound

https://huagongshe.com/reaction/748482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)-2-methyl-1,3-thiazoleHCID 736341—
ReactantHCID 3008911HCID 3008911—
Reactant1-Methyl-1H-indol-7-amineHCID 45078948—
ReactantHCID 68810405HCID 68810405—
ProductHCID 59750622HCID 59750622—

Reaction Steps

It is prepared from (2,6-dimethyl-phenyl)-[4′-methyl-4-(1-methyl-1H-indol-7-ylamino)-[1,4′]bipiperidinyl-1′-yl]-methanone and 4-chloromethyl-2-methyl-thiazole using a procedure as described for Example 52 of PCT/EP02/03871. MS/ESI 570 [M+H]+. (2,6-Dimethyl-phenyl)-[4′-methyl-4-(1-methyl-1H-indol-7-ylamino)-[1,4′]bipiperidinyl-1′-yl]-methanone used as starting material may be prepared from 1′-(2,6-dimethyl-benzoyl)-4′-methyl-[1,4′]bipiperidinyl-4-one and 1-methyl-1H-indol-7-ylamine using a procedure as described in Example 51e of PCT/EP02/03871. MS/ESI 459 [M+H]+. 1′-(2,6-Dimethyl-benzoyl)-4′-methyl-[1,4′]bipiperidinyl-4-one may be prepared using a procedure as described in Example 51a-d of PCT/EP02/03871. MS/ESI 329 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399771B2
Source datasetuspto-grants-2008_07
ORD IDord-81a09ff3b93c445789d2ef95d2a488bd
Source noteuspto-grants-2008_07