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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704078Generated: October 30, 2026

Piperidine-1-propylamine → HCID 15713319, compound

https://huagongshe.com/reaction/704078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidine-1-propylamineHCID 19049—
Reactant1-Chloro-4-methylpyridazino[4,5-b]indolizineHCID 15713312—
ProductHCID 15713319HCID 15713319—

Reaction Steps

Following the procedure of Example 1, reaction of one equivalent of 1-chloro-4-methylpyridazino[4,5-b]indolizine and 10 equivalents of 1-(3-aminopropyl)piperidine at 130° C. gave the title compound as the free base (oil, 83%) after HPLC purification. Trituration with hexane gave a yellow solid (50%), mp 130°-134° C. The free base was then converted to the dihydrochloride salt (MeOH/ethereal HCl/diethyl ether), mp. 302°-303° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985560
Source datasetuspto-grants-1991_01
ORD IDord-a84022cdbf1c41aa84ff0e60701b1e39
Source noteuspto-grants-1991_01