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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173108Generated: October 31, 2026

Hydrochloric Acid → HCID 71164946, compound

https://huagongshe.com/reaction/2173108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 71164906HCID 71164906—
SolventIsopropanolHCID 3776—
ProductHydrochloric AcidHCID 313—
ProductHCID 71164946HCID 71164946102.8%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of tert-butyl 6-(((1R,2S)-2-((tert-butoxycarbonyl)amino)cyclo-hexyl)amino)-7-fluoro-4-(5-methylpyrazolo[1,5-a]pyridin-3-yl)-3-oxo-1H-pyrrolo[3,4-c]pyridine-2(3H)-carboxylate (110 mg, 0.185 mmol) in isopropanol (10 mL) at 65° C. was added concentrated HCl (0.268 mL, 3.21 mmol) dropwise. The reaction mixture was stirred at 65° C. overnight and then slowly cooled. The solids were filtered and dried to give an HCl salt of the title compound as a pale yellow solid (75 mg, 94%). 1H NMR (500 MHz, DMSO-d6) δ ppm 1.49 (br s, 1H) 1.61-1.82 (m, 1H) 1.96 (d, J=8.79 Hz, 1H) 2.44 (s, 3H), 4.33-4.45 (m, 2H) 6.81 (d, J=6.35 Hz, 1H) 6.88 (dd, J=7.02, 1.83 Hz, 1H) 7.90 (br s, 2H) 8.20 (s, 1H) 8.37 (s, 1H) 8.66 (d, J=7.02 Hz, 1H) 9.33 (s, 1H). [M+H] calc'd for C21H23FN6O, 395. found, 395.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056873B2
Source datasetuspto-grants-2015_06
ORD IDord-81695e6dcf974f418535b8f2f83955da
Source noteuspto-grants-2015_06