HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903122Generated: November 2, 2026
Diisopropylethylamine → HCID 13136253, compound
https://huagongshe.com/reaction/1903122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Amino-4-methyl-beta-carboline-3-carboxylic-acid-ethylester | HCID 13037338 | — |
| Reactant | HCID 86614758 | HCID 86614758 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13136253 | HCID 13136253 | — |
Reaction Steps
3.25 g of 6-amino-4-methyl-beta-carboline-3-carboxylic-acid-ethylester in 70 ml of ethanol, together with 1.7 ml of 1,4-dichloro-2-cis-butene and 4.5 g of ethyldiisopropylamine is heated for 10 h at 50° C. After stirring in 250 ml of ice water, the precipitate is filtered, washed and dried in vacuum. The raw product (3.4 g of a mixture of dihydropyrrole derivative and pyrrole derivative) is dissolved in 600 ml of methylene chloride and, after addition of 17 g of pyrolusite, is stirred for 2 h at a room temperature. After filtering, and distilling off the solvent, 2.75 g of raw product is obtained crystallizing out of acetone. In this manner, 2.13 g of 4-methyl-6-(1-pyrrolyl)-beta-carboline-3-carboxylic-acid-ethylester with a m.p. of 214°-217° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04435403 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-c555992b3966494f871e7c9b99e7fcba |
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| Source note | uspto-grants-1984_03 |
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