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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354645Generated: October 31, 2026

1,4-Dioxane hydrochloride → HCID 135681563, compound

https://huagongshe.com/reaction/1354645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 135553465HCID 135553465—
SolventMethanolHCID 887—
ProductHCID 135681563HCID 13568156363%

Reaction Steps

To a solution of (±)-4-[1-(2-{4-[2-(3-chloro-phenyl)-2-hydroxy-ethylamino]-2-oxo-1,2-dihydro-pyridin-3-yl}-7-methyl-3H-benzimidazol-5-yl)-methanoyl]-piperazine-1-carboxylic acid tert-butyl ester (40 mg, 0.06 mmol) in methanol (5 mL) was added 4.0 M HCl dioxane solution (0.1 mL, excess). The reaction mixture was stirred at room temperature for 14 h. After concentration, the residue was purified by prep. HPLC to give the title compound (16 mg, 63%) as a white foam. 1H NMR (300 MHz, CD3OD) δ 7.56 (1H, s), 7.53 (1H, s), 7.23–7.41 (4H, m), 7.17 (1H, m), 6.26 (1H, d, J=7.6 Hz), 4.99 (1H, dd, J=4.7, 6.4 Hz), 3.91 (4H, broad s), 3.74 (1H, dd, J=4.7, 13.5 Hz), 3.65 (1H, dd, J=6.4, 13.5 Hz), 3.31 (4H, broad s), 2.63 (3H, s). LCMS (M+H)+ m/z 507 (t=1.38 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223757B2
Source datasetuspto-grants-2007_05
ORD IDord-3107629a00be4b45965225d0c044df00
Source noteuspto-grants-2007_05