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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292065Generated: October 30, 2026

Benzyloxyacetyl chloride → HCID 54400812, compound

https://huagongshe.com/reaction/1292065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxyacetyl chlorideHCID 177085—
ReactantMethyl indolizine-2-carboxylateHCID 600232—
ProductHCID 54400812HCID 54400812—

Reaction Steps

Following the procedure of Example 3, 2-carbomethoxyindolizine was reacted with benzyloxyacetyl chloride to give 3-benzyloxyacetyl-2-carbomethoxyindolizine (VII) Cyclization of VII with hydrazine and reaction of the resulting pyridazino[4,5-b]indolizin-1-one with POCl3 gave the corresponding chloro compound (VIII). The reaction of VII with 4-(2-pyrimidinyl)-1-piperizinyl)ethyl amine gave the title compound. Treatment with ethereal HCl in ether gave the product as the trihydrochloride salt: m.p. 140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756501
Source datasetuspto-grants-1998_05
ORD IDord-30602f6bc90742fd9f7a2ddf5b7cbc7e
Source noteuspto-grants-1998_05