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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925478Generated: October 29, 2026

Pyridine → HCID 136162347, compound

https://huagongshe.com/reaction/925478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 178483580HCID 178483580—
SolventDimethylformamideHCID 6228—
ProductHCID 136162347HCID 136162347—

Reaction Steps

500 mg (1.18 mmol) of 1-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]-benzyl}-N-hydroxy-6-oxo-1,6-dihydropyridazine-3-carboxamidine are dissolved in 15 ml of DMF, and 286 μl (3.54 mmol) of pyridine are added. 124 μl (1.30 mmol) of ethyl chloroformate are subsequently added with stirring, and the solution is stirred at 80° C. for 15 and subsequently at 100° C. for 72 h. The reaction mixture is evaporated, and the residue is purified by means of preparative HPLC; yield: 21.2 mg of “A227” trifluoroacetate; HPLC: Rt=2.07 min; LC-MS: 450 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284300B2
Source datasetuspto-grants-2016_03
ORD IDord-60f0b3d03cdf4b7781fed433bf912c53
Source noteuspto-grants-2016_03