HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972287Generated: October 31, 2026
Cyclohexanecarbonyl chloride → HCID 86645373, compound
https://huagongshe.com/reaction/1972287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86645372 | HCID 86645372 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86645373 | HCID 86645373 | — |
Reaction Steps
(S)-3-(3-(4-chlorophenyl)-2-oxo-4-(3-(trifluoromethyl)phenyl)-imidazolidin-1-yl)-N′-hydroxypropanimidamide (28.7 mg, 0.067 mmol) is dissolved in dichloromethane (2 mL). Cyclohexanecarbonyl chloride (14.8 mg, 0.10 mmol) and diisopropyl ethylamine (26.3 mg, 0.20 mmol) are then added. The reaction is stirred for 3 h at room temperature. The reaction is diluted with ethyl acetate followed by quenching with sat. sodium bicarbonate solution. The organic layer is washed with brine and dried with MgSO4. The solvents is removed under vacuum to afford crude (S)-3-(3-(4-chlorophenyl)-2-oxo-4-(3-(trifluoromethyl)phenyl)imidazolidin-1-yl)-N′-(cyclohexanecarbonyloxy)propanimidamide which is used directly in the next step without further purification. HPLC-MS calculated for C26H29ClF3N4O3 (M+H+) 537.1, found 537.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431607B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-e3346f16a76745fca32004d87117bb01 |
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| Source note | uspto-grants-2013_04 |
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