HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648567Generated: October 27, 2026
Hydrochloric Acid → Ethyl 2-amino-5-(2-pyridinecarbonyl)-4-thiazolecarboxylate
https://huagongshe.com/reaction/648567
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl 3-chloro-4-(2-pyridyl)-2,4-dioxo-butyrate hydrochloride | HCID 20144948 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-amino-5-(2-pyridinecarbonyl)-4-thiazolecarboxylate | HCID 20145044 | 20.7% |
Reaction Steps
To a solution of thiourea (4.5 g) and sodium acetate (5 g) in a mixture of tetrahydrofuran (50 ml) and water (15 ml) was added ethyl 3-chloro-4-(2-pyridyl)-2,4-dioxo-butyrate hydrochloride (5.6 g). After the mixture was stirred at 45° C. to 50° C. for 2 hours, water (50 ml) was added thereto. The resulting mixtures was acidified to pH 1.0 with 10% hydrochloric acid. The precipitate was collected by filtration. The precipitate was added to a mixture of water and ethyl acetate, and adjusted to pH 6.0 with 10% potassium carbonate. The separated ethyl acetate layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was recrystallized from a mixture of ethyl acetate and tetrahydrofuran to give ethyl 2-amino-5-(2-pyridinecarbonyl)-4-thiazolecarboxylate (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04735957 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-1e5ee50e2c5b46098b2e1f80f7594485 |
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| Source note | uspto-grants-1988_04 |
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