HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423384Generated: November 1, 2026
Hydrochloric Acid → HCID 178470387, compound
https://huagongshe.com/reaction/1423384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Ethyl 3-amino-5-methyl-1H-pyrrole-2-carboxylate | HCID 24754830 | — |
| Product | HCID 178470387 | HCID 178470387 | — |
Reaction Steps
Ethyl-3-amino-5-methyl-1H-pyrrole-2-carboxylate (58.87 g; 0.35 mol) prepared according to literature [Gangjee A.; Li W.; Yang J.; Kisliuk R. L.; J. Med. Chem. 2008, 51, 68] is suspended in acetonitrile (1750 mL). To the suspension is added dropwise 4M HCl in dioxane (473 mL; 1.89 mol) within 15 minutes. After complete addition the reaction mixture is heated to 50° C. for 18 hours. The reaction mixture is cooled to 10° C., the solid is collected by suction filtration and washed with cold acetonitrile (400 mL). A second crop of product is obtained from the mother liquor after concentration under reduced pressure. The residue is collected with t-butylmethyl-ether. After the suction filtration the solids are combined and dried in vacuum at 50° C. to yield the title compound as off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927557B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-01b4e04b164f4f768ab160362b20d63a |
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| Source note | uspto-grants-2015_01 |
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