Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271807Generated: November 1, 2026

Hydrochloric Acid → HCID 178467111, compound

https://huagongshe.com/reaction/2271807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantHCID 178467113HCID 178467113—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178467111HCID 17846711159%

Reaction Steps

To a suspension of tert-butyl (trans-4-((3-acetyl-6-(3-chloro-5-fluoro-4-hydroxyphenyl)quinolin-4-yl)amino)cyclohexyl)carbamate (38 mg, 0.072 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 purified by preparative HPLC (C18 silica, 10-90% methanol/water with 0.05% TFA). The residue was eluted through an ion-exchange column (using methanol and 7 N methanol in ammonia) to obtain the desired product (18.1 mg, 59%) as a yellow solid. 1H NMR (500 MHz, MeOD+TFA-d) δ 9.12 (s, 1H), 8.47 (s, 1H), 8.32-8.26 (m, 1H), 7.99 (d, J=8.7 Hz, 1H), 7.59 (s, 1H), 7.52 (d, J=11.5 Hz, 1H), 4.57-4.53 (m, 1H), 2.74 (s, 3H), 2.51 (d, J=12.3 Hz, 2H), 2.26 (d, J=12.3 Hz, 2H), 1.87 (q, J=12.5 Hz, 2H), 1.71-1.62 (m, 2H). ESI MS m/z 428 [C23H23ClFN3O2+H]+; HPLC>99% (AUC), tR=9.43 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-b31d1e745e5a4a28b9d68107c9329573
Source noteuspto-grants-2015_09