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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640421Generated: October 28, 2026

3-Chloro-6-(1-piperazinyl)pyridazine → HCID 60209564, compound

https://huagongshe.com/reaction/1640421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-(1-piperazinyl)pyridazineHCID 5294926—
ReactantEthyl [(phenoxycarbonyl)oxy]acetateHCID 12094709—
ProductHCID 60209564HCID 60209564—

Reaction Steps

The process is performed as described in Example 1 (step 1.2.). Starting with 1.60 g (8.05 mmol) of 3-chloro-6-(1-piperazinyl)pyridazine (J. Med. Chem., 18, 2002, 4011-4017) and 1.99 g (8.86 mmol) of ethyl [(phenyloxycarbonyl)oxy]acetate, prepared in step 1.1. of Example 1, and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 1.70 g of product are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114866B2
Source datasetuspto-grants-2012_02
ORD IDord-ffe7d0981553432fba74ce078f815d79
Source noteuspto-grants-2012_02