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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476647Generated: November 1, 2026

Hydrochloric Acid → 6-(1,3-benzodioxol-5-yl)-1-[(3-ethyl-1,2,4-oxadiazol-5-yl)methyl]-3-(piperidin-4-yl)thieno[3,2-d]pyrimidine-2,4(1H,3H)-dione hydrochloride

https://huagongshe.com/reaction/1476647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-butyl 4-[6-(1,3-benzodioxol-5-yl)-1-[(3-ethyl-1,2,4-oxadiazol-5-yl)methyl]-2,4-dioxo-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl]piperidine-1-carboxylateHCID 67258594—
Solvent1,4-DioxaneHCID 31275—
Product6-(1,3-benzodioxol-5-yl)-1-[(3-ethyl-1,2,4-oxadiazol-5-yl)methyl]-3-(piperidin-4-yl)thieno[3,2-d]pyrimidine-2,4(1H,3H)-dione hydrochlorideHCID 67259192—

Reaction Steps

To a solution of tert-butyl 4-[6-(1,3-benzodioxol-5-yl)-1-[(3-ethyl-1,2,4-oxadiazol-5-yl)methyl]-2,4-dioxo-1,4-dihydrothieno[3,2-d]pyrimidin-3(2H)-yl]piperidine-1-carboxylate (3.75 g; compound B64) in 1,4 dioxane (130 ml) is added a solution of hydrogen chloride in 1,4-dioxane (31 ml, 4.0 M). The reaction mixture is stirred for 12 h at RT. To complete the reaction an additional amount of a solution of hydrogen chloride in 1,4-dioxane (5.0 ml, 4.0 M) is added and the mixture is stirred for 20 h at RT. Subsequently the suspension is filtered to give title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018175B2
Source datasetuspto-grants-2015_04
ORD IDord-6e03f2c8fecf4324af284d7d922030c5
Source noteuspto-grants-2015_04