Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | HCID 20780216 | HCID 20780216 | — |
| Catalyst | Silver(I) trifluoromethanesulfonate | HCID 76223 | — |
| Product | HCID 21916253 | HCID 21916253 | — |
Reaction Steps
A suspension of 2-bromo-5-trifluoromethyl-3-[(2,4,6-trimethyl-phenylcarbamoyl)-methyl]-3H-imidazole-4-carboxylic acid ethyl ester (20.12 g, 0.044 mmol) and silver triflate (11.87 g, 0.046 mol) in sulfolane (200 mL) was heated at 150° C. for 6 h. The resulting reaction mixture was cooled to room temperature and filtered through a short pad of celite. The final purification was achieved by a reverse-phase preparative HPLC to give the desired product as yellowish solid. Yield−5.24 g (24%). LC/MS: tR=1.89 min., MS: [M+H]=382. 6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)-7H-imidazo[1,2-a]imidazole-3-carboxylic acid ethyl ester, scheme 6: (AA)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06888004B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-e50b5c80fbfd4088878502a9bf76f6a5 |
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| Source note | uspto-grants-2005_05 |
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