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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713902Generated: October 30, 2026

Hydrochloric Acid → HCID 178445773, compound

https://huagongshe.com/reaction/713902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178471605HCID 178471605—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178445773HCID 178445773—

Reaction Steps

To a solution of ethyl 4-((6-((trans)-4-tert-butylcyclohexyloxy)-5-(trifluoromethyl)naphthalen-2-yl)methylamino)butanoate (150 mg, 0.30 mmol) in THF (15 mL) was added 1M HCl 93 mL) and refluxed for 1 h. Then the reaction was concentrated to give 4-((6-((trans)-4-tert-butylcyclohexyloxy)-5-(trifluoromethyl)naphthalen-2-yl)methylamino)butanoic acid as a white solid, purified by HPLC-preparation (0.05% TFA/water: MeOH=0˜95%), 50 mg, white solid (yield: 34%). ESI-MS (M+H+): 466.3 HPLC: 96.13%. 1H NMR (400 MHz, CD3OD) δ: 8.20 (d, 1H), 8.10 (d, 1H), 8.01 (d, 1H), 7.65 (dd, 1H), 7.57 (d, 1H), 4.50-4.46 (m, 1H), 4.34 (s, 2H), 3.16 (t, 2H), 2.46 (d, 2H), 2.21 (d, 2H), 1.98 (t, 2H), 1.90 (d, 2H), 1.49 (q, 2H), 1.25 (q, 2H), 1.14-1.08 (m, 1H), 0.91 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186367B2
Source datasetuspto-grants-2015_11
ORD IDord-29f63a279c37454b8973039e36ec70b6
Source noteuspto-grants-2015_11