HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660133Generated: October 31, 2026
Hydrochloric Acid → HCID 178522244, compound
https://huagongshe.com/reaction/660133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | O,O-Dipyridin-2-yl carbonothioate | HCID 719784 | — |
| Reactant | 3-Amino-5-fluorobenzotrifluoride | HCID 2735913 | — |
| Reactant | HCID 178472469 | HCID 178472469 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178522244 | HCID 178522244 | 44.1% |
Reaction Steps
Sodium hydride (60% dispersion in mineral oil, 192 mg, 4.80 mmol) was added to a stirred solution of 3-amino-5-fluorobenzotrifluoride (430 mg, 2.40 mmol) in DMF (10 mL) at ambient temperature. After 5 mins di-2-pyridyl thionocarbonate (557 mg, 2.40 mmol) was added in one portion and stirring was continued for 10 mins. Ethyl cis-4-(4-{[hydrazino(oxo)acetyl]amino}phenoxy)cyclohexanecarboxylate (Intermediate 1, 698 mg, 2.00 mmol) was added in one portion to the reaction mixture and stirred at 65° C. for 30 mins. EDCI (460 mg, 2.40 mmol) was then added in one portion and the reaction mixture was heated to 85° C. for 3 h. The mixture was cooled to ambient temperature and water (15 mL) was added and the resulting suspension was filtered to leave a cream solid. The solid was taken up in a mixture of MeOH (8 mL) and THF (4 mL) and a 2N aqueous solution of NaOH (4 mL) was added in one portion and the reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was acidified by the addition of 2M HCl and the resulting precipitate was filtered, washed with water (10 mL) and dried under high vacuum to leave a solid. The solid was recrystallised from refluxing glacial acetic acid to provide the title compound as a white solid (448 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084478B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-dc311c494aa1429083189bf23d9a43fe |
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| Source note | uspto-grants-2011_12 |
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