HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507542Generated: October 26, 2026
Methane → 5-Bromo-2-(methylthio)pyrimidine-4-carboxylic Acid
https://huagongshe.com/reaction/507542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methyl-2-thiopseudourea sulfate | HCID 75270 | — |
| Reactant | Mucobromic Acid | HCID 3033972 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-2-(methylthio)pyrimidine-4-carboxylic Acid | HCID 291786 | 59.1% |
Reaction Steps
Mucobromic acid (58.05 g, 0.225 mol) was added to a stirred solution of 2-methyl-2-thio-pseudourea sulfate (62.66 g, 0.225 mol) in water (500 mL) at r.t. The suspension was cooled to 10° C. (ice bath) and triethylamine (94.1 mL, 0.675 mol) was added dropwise over 4 h. The reaction mixture was then left to stand at r.t. for 24 h. Activated carbon (Darco G-60) was added to the now dark red/brown solution and after stirring for 10 min the charcoal was filtered off. The filtrate was acidified with concentrated hydrochloric acid (50 mL) and the yellow precipitate was filtered off, washed with water (2×80 mL) and diethyl ether (2×100 mL), and then placed in a vacuum oven at 50° C. for 2 days to yield 5-bromo-2-(methylthio)pyrimidine-4-carboxylic acid (33.13 g, 59%) as a yellow amorphous solid. 1H NMR δ (d6-DMSO, 400 MHz) 2.75 (s, 3H), 9.20 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786132B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-24445af16d2140b887645c7414873057 |
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| Source note | uspto-grants-2010_08 |
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