HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795952Generated: November 3, 2026
Hydrochloric Acid → HCID 135752502, compound
https://huagongshe.com/reaction/1795952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 22180042 | HCID 22180042 | — |
| Product | HCID 135752502 | HCID 135752502 | 64% |
Reaction Steps
A mixture of methyl 1-amino-5-chloro-1H-pyrrole-2-carboxylate hydrochloride (Example 13 A, 2.2 g, 9.8 mmol) and 4 N HCl in dioxane (6.0 mL, 24 mmol) in acetonitrile (90 mL) was placed in a sealed tube and heated at 82° C. overnight. The reaction mixture was concentrated and diluted with fresh acetonitrile (100 mL) and triethylamine (5 mL). The reaction mixture was heated at 85° C. overnight, concentrated to dryness and diluted with EtOAc to 150 mL. The EtOAc solution was washed with 1 N HCl, followed by saturated NaHCO3 solution and brine. The solution was dried over MgSO4 and concentrated to a solid. The solid was triturated with Et2O/hexane to give the title compound as a brown solid (1.15 g, 64%): 1H NMR (CDCl3) δ 6.99 (d, 1H, J=4.38 Hz), 6.42 (d, 1H, J=4.38 Hz), 2.40 (s, 3H); MS (ESI+) 183.98, 185.97 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030118B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-582a7c75d28b42b297df5ad9e7d29039 |
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| Source note | uspto-grants-2006_04 |
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