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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037349Generated: November 1, 2026

Hydrochloric Acid → HCID 68227563, compound

https://huagongshe.com/reaction/1037349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-[4-(1-Amino-cyclobutyl)-phenyl]-6-fluoro-2-phenyl-chromen-4-oneHCID 51030598—
ReactantHCID 67067856HCID 67067856—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 68227563HCID 6822756385%

Reaction Steps

Following the procedure used to prepare 3-[4-(1-amino-cyclobutyl)-phenyl]-6-fluoro-2-phenyl-chromen-4-one, {1-[4-(1-ethyl-6-oxo-8-phenyl-1,6-dihydro-9-oxa-1,2-diaza-cyclopenta[a]naphthalen-7-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester was treated with TFA. The resultant free base was dissolved in a mixture of MeOH (1.5 mL), water (3.5 mL) and 1 M HCl (0.2 mL) and chromatographed on a 5 g C18 cartridge {gradient 30 to 70% MeOH in water+1 M HCl (60 μL in each 10 mL of eluent)} to give the title compound (33 mg, 85%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 8.46 (br s, 3H), 8.30 (s, 1H), 7.82 (d, J=8.6 Hz, 1H), 7.75 (d, J=8.5 Hz, 1H), 7.54-7.38 (m, 7H), 7.32 (d, J=8.3 Hz, 2H), 4.77 (q, J=7.2 Hz, 2H), 2.62-2.49 (m, 4H), 2.23-2.12 (m, 1H), 1.86-1.75 (m, 1H), 1.47 (t, J=7.2 Hz, 3H). LCMS (Method E): RT=3.58 min, [M+H]+=436.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-cd20a14df52b4b7c9f9a3ed8f7fe50b8
Source noteuspto-grants-2013_10