HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255076Generated: October 25, 2026
Triethylamine → Adamantane-1-carboxylic acid (5-chloro-thiazol-2-yl)-amide
https://huagongshe.com/reaction/255076
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-5-chlorothiazole | HCID 38942 | — |
| Reactant | 1-Adamantanecarbonyl chloride | HCID 98915 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Adamantane-1-carboxylic acid (5-chloro-thiazol-2-yl)-amide | HCID 86619048 | 51.3% |
Reaction Steps
A mixture of 2-amino-5-chlorothiazole (2.00 g, 14.9 mmol), 1-adamantanecarbonyl chloride (3.54 g, 17.8 mmol), 4-dimethylaminopyridine (1.10 g, 0.90 mmol) and triethylamine (4.15 mL, 23.0 mmol) in 80 mL of THF was stirred at 80° C. for 48 hours The mixture was cooled to ambient temperature, diluted with 100 mL of ethyl acetate and washed with brine. The layers were separated and the aqueous phase was extracted twice with 50 mL of ethyl acetate. The combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated. Purification by column chromatography (SiO2, dichloromethane) afforded 2.27 g of the title compound: MS (DCI/NH3) m/z 297 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875639B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-db9f264b210b4ee888b9dfde0a1eb5e9 |
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| Source note | uspto-grants-2011_01 |
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