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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 135553465 | HCID 135553465 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135681563 | HCID 135681563 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07223757B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-3107629a00be4b45965225d0c044df00 |
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| Source note | uspto-grants-2007_05 |
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