HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515250Generated: October 25, 2026
Hydrochloric Acid → Methyl 2-(6-bromo-2-methylpyrimidin-4-ylamino)thiazole-5-formate
https://huagongshe.com/reaction/515250
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-chloro-1,3-thiazole-5-carboxylate | HCID 12897294 | — |
| Reactant | 4-Amino-6-bromo-2-methylpyrimidine | HCID 56965719 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(6-bromo-2-methylpyrimidin-4-ylamino)thiazole-5-formate | HCID 49821806 | 78.4% |
Reaction Steps
60% sodium hydride (12.0 g, 0.30 mol) was suspended in THF (300 mL) and cooled down to 0° C. 4-amino-6-bromo-2-methylpyrimidine (Compound 9) (18.7 g, 0.1 mol) was then added in batches and stirred for 30 min. After methyl 2-chlorothiazole-5-formate (Compound 10) (17.7 g, 0.1 mol) was added in batches, the reactants were heated and reacted by refluxing for 4 h, and then cooled down to room temperature for reaction overnight. When controlling the temperature between 0° C. and 5° C., hydrochloric acid (2N) was added for neutralization reaction. After adding keep heat and stirred to grow grains for 1 h. Filtrate and wash the cake with water, and then dry to give target Compound 11 (25.8 g, yield is 78.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108954B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-5b795298847a425e8aeb14da61765404 |
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| Source note | uspto-grants-2015_08 |
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