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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969914Generated: October 30, 2026

Hydrochloric Acid → HCID 68455869, compound

https://huagongshe.com/reaction/969914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 68455870HCID 68455870—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 68455869HCID 6845586974%

Reaction Steps

To a solution of (S)-N-(1-azabicyclo[2.2.2]oct-3-yl)-2-(4-methylthiazol-5-yl)benzoxazole-4-carboxamide (45 mg, 0.12 mmol) in methanol (2.0 mL) was added a solution of HCl in diethyl ether (1 N, 1.5 mL, 1.5 mmol) at room temperature slowly. The reaction mixture was diluted with diethyl ether. The resulting solid was filtered and washed with diethyl ether to afford (S)-N-(1-azabicyclo[2.2.2]oct-3-yl)-2-(4-methylthiazol-5-yl)benzoxazole-4-carboxamide hydrochloride (40 mg, 74%) as a light yellow solid: 1H NMR (500 MHz, DMSO-d6) δ 10.46 (s, 1H), 9.35 (s, 1H), 9.10 (d, J=6.3 Hz, 1H), 8.05 (dd, J=8.2, 0.9 Hz, 1H), 7.94 (dd, J=7.7, 0.9 Hz, 1H), 7.58 (t, J=8.0 Hz, 1H), 4.44-4.40 (m, 1H), 3.64-3.55 (m, 1H), 3.35-3.15 (m, 5H), 2.91(s, 3H), 2.33-2.25 (m, 2H), 2.00-1.95 (m, 3H); MS (ESI+) m/z 369 (M+H); HPLC>99% (AUC), tR=12.05 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307094B2
Source datasetuspto-grants-2007_12
ORD IDord-a9fbdba9e3964d759b91f2bff66d16fd
Source noteuspto-grants-2007_12