HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652059Generated: October 31, 2026
Pyridine → 1,3-Dimethyl-5-ethoxycarbonyl-2-thiobarbituric acid
https://huagongshe.com/reaction/652059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1,3-Dimethyl-2-sulfanylidene-1,3-diazinane-4,6-dione | HCID 598948 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,3-Dimethyl-5-ethoxycarbonyl-2-thiobarbituric acid | HCID 14053347 | — |
Reaction Steps
155 g (0.9 mol) of 1,3-dimethyl-2-thiobarbituric acid, 88,3 g (1.12 mol) of pyridine and 9 g of 4-dimethylaminopyridine are dissolved in 660 ml of dichloromethane and the solution is cooled to 0° C. Then 102 g (0.94 mol) of ethyl chloroformate are added dropwise over 1 hour. The mixture is subsequently stirred for 12 hours at 0° C., then allowed to warm to room temperature and worked up after a further 7 hours as follows. 600 ml of dichloromethane are added and the solution is washed with three 1000 ml portions of water, dried over Na2SO4 and the solvent is evaporated off. The crude product is recrystallised from ethanol. Melting point 90°-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670441 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-764a040fd5764919b72eaf4c17c1917f |
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| Source note | uspto-grants-1987_06 |
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