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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648728Generated: October 30, 2026

HCID 12798005, compound → HCID 21243579, compound

https://huagongshe.com/reaction/648728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12798005HCID 12798005—
Reactant4-hydroxy-1H-indole-3-carbonitrileHCID 13186949—
ReactantHCID 21243576HCID 21243576—
ProductHCID 21243579HCID 21243579—

Reaction Steps

Compounds of general formula (I) can be further reacted by known methods, for example by saponification and decarboxylation to give 4-hydroxyindole or 4-hydroxy-6-methylindole, or by aminolysis and dehydration to give 4-hydroxy-3-cyanoindole or 4-hydroxy-3-cyano-6-methylindole, which, by reaction with epichlorohydrin and alkylamino derivatives, give aminopropanols with useful pharmacological properties (see Federal Republic of Germany Patent Specification Nos. 25 08 251; 27 37 630; 29 05 877 and 30 30 047). However, compounds of general formula (I) can also be reacted to give aminopropanol derivatives directly, whereafter the compounds obtained are subsequently changed. Thus, for example, from 4-hydroxy-3-cyanoindole (see Federal Republic of Germany Patent Specification No. 30 29 980) there is obtained 4-(2,3-epoxypropoxy)-3-cyanoindole which is reacted with 2-(2-allyloxyphenoxy)-ethylamine to give the pharmacologically effective 4-{2-hydroxy-3-[2-(2-allyloxyphenoxy)-ethylamino]-propoxy}-3-cyanoindole (see Example 3h) of Federal Republic of Germany Patent Specification No. 30 30 047).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736043
Source datasetuspto-grants-1988_04
ORD IDord-4577b4544e734d2d92b05c3367a2514d
Source noteuspto-grants-1988_04