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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196609Generated: October 30, 2026

1-(3-Bromopropyl)pyrrolidine hydrobromide → N-(3-methyl-1,2,4-thiadiazol-5-yl)-6-[(4-methyl-4H-1,2,4-triazol-3-yl)thio]-3-{[4-(3-pyrrolidin-1-ylpropoxy)phenyl]thio}pyridine-2-carboxamide

https://huagongshe.com/reaction/2196609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Bromopropyl)pyrrolidine hydrobromideHCID 20135920—
Reactant3-[(4-hydroxyphenyl)thio]-N-(3-methyl-1,2,4-thiadiazol-5-yl)-6-[(4-methyl-4H-1,2,4-triazol-3-yl)thio]pyridine-2-carboxamideHCID 59706252—
ProductN-(3-methyl-1,2,4-thiadiazol-5-yl)-6-[(4-methyl-4H-1,2,4-triazol-3-yl)thio]-3-{[4-(3-pyrrolidin-1-ylpropoxy)phenyl]thio}pyridine-2-carboxamideHCID 2506640016.9%

Reaction Steps

Using 19 mg of 3-[(4-hydroxyphenyl)thio]-N-(3-methyl-1,2,4-thiadiazol-5-yl)-6-[(4-methyl-4H-1,2,4-triazol-3-yl)thio]pyridine-2-carboxamide obtained in Reference Example (step 3) and 13 mg of 1-(3-bromopropyl)pyrrolidine hydrobromide obtained in the step 1, 4 mg of the entitled compound was obtained as a pale yellow solid in the same method as in Example 2 or in accordance with the method or by combining it with an ordinary method.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338460B2
Source datasetuspto-grants-2012_12
ORD IDord-cc87139ad82f446b95ccc30fbfc27d3c
Source noteuspto-grants-2012_12