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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663927Generated: October 31, 2026

Tetrahydrofuran → HCID 57505664, compound

https://huagongshe.com/reaction/1663927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Butynoic acidHCID 68535—
ReactantN-{5-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide hydrochlorideHCID 57505635—
CatalystDimethylformamideHCID 6228—
SolventDimethylacetamideHCID 31374—
ProductHCID 57505664HCID 5750566437%

Reaction Steps

In the same manner as in Example 279 and using but-2-ynoic acid (46 mg, 0.54 mmol), tetrahydrofuran (1.5 mL), N,N-dimethylformamide (1 drop), oxalyl chloride (47 μL, 0.54 mmol), N-{5-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide hydrochloride (150 mg, 0.36 mmol) and N,N-dimethylacetamide (5 mL) as starting materials, the title compound (60 mg, 37%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034812B2
Source datasetuspto-grants-2011_10
ORD IDord-fe5bc6e392954085a7af28113fb0a5ab
Source noteuspto-grants-2011_10