HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196806Generated: October 30, 2026
2,5-Dichlorobenzoic acid → HCID 3505448, compound
https://huagongshe.com/reaction/2196806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dichlorobenzoic acid | HCID 5784 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | 2-Amino-5-methylthiazole | HCID 351770 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 3505448 | HCID 3505448 | 79.1% |
Reaction Steps
To a solution of 5-methylthiazole-2-amine (Aldrich, 1.0 g, 8.76 mmol) in tetrahydrofuran (10 mL) was added 2,5-dichlorobenzoic acid (Aldrich) (2.01 g, 10.51 mmol), triethylamine (2.93 mL, 21.02 mmol), and 1-propanephosphonic acid cyclic anhydride (Aldrich, 50% solution in ethyl acetate, 6.19 mL, 10.51 mmol). The reaction mixture was stirred at 22° C. for 14 h., cooled, and quenched with saturated aqueous NaHCO3 (20 mL). The aqueous layer was extracted with ethyl acetate (2×40 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography using an Analogix® Intelliflash280 ™ (SiO2, 0-100% ethyl acetate in hexanes) to afford 1.99 g of the title compound. MS (ESI+) m/z 287 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338467B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-eb2e34f42ed045e6ad99c635967e0e3e |
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| Source note | uspto-grants-2012_12 |
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