HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157933Generated: November 1, 2026
Methanol → Methyl 4-amino-1,3-thiazole-5-carboxylate
https://huagongshe.com/reaction/1157933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 4-amino-2-(methylsulfonyl)thiazole-5-carboxylate | HCID 59511825 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-amino-1,3-thiazole-5-carboxylate | HCID 15832487 | 60.8% |
Reaction Steps
To a 1 l solution of 37.6 g of 4-amino-2-methanesulfonylthiazole-5-carboxylic acid methyl ester in a methanol:THF=1:1 mixed solvent at room temperature, there was gradually added 15 g of sodium borohydride over a period of 10 hours. Stirring was continued for 40 hours at room temperature, and then the reaction mixture was poured into a mixture of 6 l of ethyl acetate and 3 l of water. The organic layer was washed with 3 l of water and 3 l of brine, and the aqueous layer was extracted again with ethyl acetate. The organic layers were combined and dried over anhydrous magnesium sulfate. The desiccant was filtered out and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane system) to obtain the target compound (15.3 g) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07807690B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-9163fac127284723b83e348a5dd59efa |
|---|
| Source note | uspto-grants-2010_10 |
|---|