HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35273Generated: October 29, 2026
Hydrochloric Acid → HCID 54551545, compound
https://huagongshe.com/reaction/35273
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-[N-methyl-4-nitro-pyrrole-2-carboxamido]propyldimethylamine | HCID 54253890 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 54551545 | HCID 54551545 | — |
Reaction Steps
The compound of example 1 (3.4 g) was dissolved in ethanol (40 ml) and diluted hydrochloric acid (20 ml) and reduced over a Pd catalyst (5% on carbon) under H2 pressure (50 psi) in a Parr apparatus. Water (20 ml) was added and the catalyst filtered off. The resulting solution was concentrated and the residue was dissolved in water (40 ml). Sodium bicarbonate (4 g) was added, followed by a solution of N-methyl-4-nitropyrrole-2-carboxylic acid chloride (2.8 g) in 20 ml of benzene. The resulting mixture was stirred for about 2 hours at room temperature and then was extracted with chloroform. The dried organic extracts were concentrated in vacuo and the residue was purified by column chromatography (CHCl3 75, EtOH95% 25, NH4OH 0.6) to give 4.7 g of 3-[N-methyl-4-(N-methyl-4-nitropyrrole-2-carboxamido)pyrrole-2-carboxamido]propyl-dimethylamine as a yellow solid, m.p. 178°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766142 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-1715224bf0c540359d169445f3e1e3d2 |
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| Source note | uspto-grants-1988_08 |
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