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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497603Generated: November 1, 2026

Butyryl chloride → N-[4-iodo-1H-indazol-3-yl]butanamide

https://huagongshe.com/reaction/497603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyryl chlorideHCID 8855—
Reactant4-iodo-1H-indazol-3-amineHCID 4057787—
SolventPyridineHCID 1049—
ProductN-[4-iodo-1H-indazol-3-yl]butanamideHCID 10381892—

Reaction Conditions

Temperature5 °C

Reaction Steps

0.20 cm3 of butyryl chloride is added to 500 mg of 4-iodo-1H-indazole-3-amine, described previously, in 15 cm3 of pyridine, and cooled to about 5° C. The reaction medium is allowed to return to about 19° C. over 50 hours. The reaction medium is evaporated under reduced pressure (2 kPa; 50° C.). The residue is taken up in 15 cm3 of ethyl acetate, 15 cm3 of tetrahydrofuran and 15 cm3 of distilled water. The organic phase is dried over magnesium sulphate and then filtered through a sinter funnel and evaporated under reduced pressure (2 kPa; 50° C.). The residue is taken up in 15 cm3 of dichloromethane and filtered. The insoluble material is taken up in 10 cm3 of methanol and filtered off and the filtrate is evaporated under reduced pressure, to give after drying (90 Pa; 50° C.), 70 mg of N-[4-iodo-1H-indazol-3-yl]butanamide in the form of an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949579B2
Source datasetuspto-grants-2005_09
ORD IDord-2d51e8a6effc4221869aa3f3ffdb360f
Source noteuspto-grants-2005_09