HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648728Generated: October 30, 2026
HCID 12798005, compound → HCID 21243579, compound
https://huagongshe.com/reaction/648728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12798005 | HCID 12798005 | — |
| Reactant | 4-hydroxy-1H-indole-3-carbonitrile | HCID 13186949 | — |
| Reactant | HCID 21243576 | HCID 21243576 | — |
| Product | HCID 21243579 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04736043 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-4577b4544e734d2d92b05c3367a2514d |
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| Source note | uspto-grants-1988_04 |
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