HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696436Generated: October 26, 2026
2-Methyl-2-thiopseudourea → HCID 178418871, compound
https://huagongshe.com/reaction/1696436
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-thiopseudourea | HCID 5142 | — |
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178418871 | HCID 178418871 | 158.1% |
Reaction Steps
To a solution of 2-ethoxymethylenemalonic acid diethyl ester (59.0 g, 273 mmol) in EtOH (300 mL) was added 2-methyl-isothiourea (41.5 g, 150 mmol) in an ice-H2O bath. An EtOHic solution of EtONa (2M, 300 mL) was added dropwise maintaining the reaction temperature under 5° C. The mixture was warmed to RT and stirred for 3 h. After standing overnight, the solvent was removed under reduced pressureand the residue was dissolved in H2O (800 mL) at 0° C. The solution was acidified to pH 3 with conc. HCl and the precipitate collected by filtration and air-dried to yield 4-hydroxy-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester as a white solid (50.8 g, 87.6% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.48 (s, 1H), 4.20 (q, J=9.6 Hz, 2H), 2.51 (s, 3H), 1.23 (t, J=9.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163756B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-fd915514089444d8a0eae3c0f5d8585e |
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| Source note | uspto-grants-2012_04 |
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