HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271811Generated: November 3, 2026
Hydrochloric Acid → HCID 178450288, compound
https://huagongshe.com/reaction/2271811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 178450290 | HCID 178450290 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178450288 | HCID 178450288 | 71.2% |
Reaction Steps
To a suspension of tert-butyl (trans-4-((3-butyryl-6-(3-chloro-5-fluoro-4-hydroxyphenyl)quinolin-4-yl)amino)cyclohexyl)carbamate (36 mg, 0.065 mmol) in THF (3 mL) was added water (2 mL) and 6N aqueous HCl (2 mL). The resultant solution was heated at 65° C. for 4 h. The reaction mixture was cooled and concentrated. The resultant residue was triturated with diethyl ether. The residue was eluted through an ion-exchange column (using methanol and 7 N methanol in ammonia) to obtain the desired product (21.1 mg, 71%) as a yellow solid. 1H NMR (500 MHz, MeOD+TFA-d) δ 9.15 (s, 1H), 8.47 (s, 1H), 8.28 (dd, J=8.7, 1.8 Hz, 1H), 7.99 (d, J=8.7 Hz, 1H), 7.59 (s, 1H), 7.51 (d, J=11.4 Hz, 1H), 4.55 (br s, 1H), 3.13 (t, J=7.2 Hz, 2H), 2.53-2.49 (m, 2H), 2.26 (d, J=12.1 Hz, 2H), 1.94-1.74 (m, 4H), 1.68-1.62 (m, 2H), 1.06 (t, J=7.4 Hz, 3H). ESI MS m/z 456 [C25H27ClFN3O2+H]+; HPLC>99% (AUC), tR=10.83 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120749B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-0af027a56fe840a993fee4ac64f7a56f |
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| Source note | uspto-grants-2015_09 |
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