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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273074Generated: October 30, 2026

HCID 68576037, compound → HCID 59837523, compound

https://huagongshe.com/reaction/273074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68576037HCID 68576037—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductAmmoniaHCID 222—
ProductHCID 59837523HCID 5983752377.2%

Reaction Steps

4-{4-[4-(3-[1,4]Oxazepan-4-yl-propoxy)-phenyl]-tetrahydro-pyran-4-carbonyl}-piperazine-1-carboxylic acid tert-butyl ester (260 mg, 0.48 mmol) was dissolved in a solution of hydrogen chloride in dioxane (4M, 5 ml) and was stirred at room temperature for 2 hours. The solvent was removed in vacuo and the residue dissolved in DCM (10 ml) and washed with saturated sodium bicarbonate solution (15 ml). The organic layer was dried over Na2SO4 and concentrated in vacuo before purifying the residue using column chromatography, eluting with a gradient of DCM:MeOH:NH3 (from 99:1:0.1 to 92:8:0.8) to afford the title compound as a white solid (80 mg, 37%). 1H NMR (400 MHz, d6-DMSO) δ 1.70-1.88 (m, 6H), 2.08 (m, 2H), 2.52-2.63 (m, 6H), 3.04-3.35 (m, 8H), 3.58 (m, 4H), 3.64 (m, 2H), 3.72 (m, 2H), 3.98 (t, 2H), 6.92 (d, 2H), 7.12 (d, 2H). LRMS ESI+ m/z 432 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456164B2
Source datasetuspto-grants-2008_11
ORD IDord-fbe480f34c1044e5911b20596c2e8090
Source noteuspto-grants-2008_11