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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454946Generated: October 30, 2026

Ammonium Carbonate → HCID 67523147, compound

https://huagongshe.com/reaction/1454946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium CarbonateHCID 517111—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 66754105HCID 66754105—
ReactantHCID 178418300HCID 178418300—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 67523147HCID 67523147—

Reaction Steps

A mixture of 250 mg of 1-[2-(2-carboxy-phenyl)-2-oxo-ethyl]-3-methyl-7-(3-methyl-2-buten-1-yl)-8-[3-(tert.-butyloxycarbonyl-amino)-piperidin-1-yl]-xanthine, 404 mg of ammonium carbonate, 135 mg of O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium-tetrafluoroborate, 57 mg of hydroxybenzotriazole and 59 μl of triethylamine in 3 ml of tetrahydrofuran is stirred for eight hours at ambient temperature. For working up the reaction mixture is diluted with 30 ml of ethyl acetate and washed with 10% citric acid solution, 10% potassium carbonate solution and saturated sodium chloride solution. The organic phase is evaporated down and chromatographed through a silica gel column with methylene chloride/methanol (98:2 to 80:20).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482337B2
Source datasetuspto-grants-2009_01
ORD IDord-32e261ca51d1466c904c6f4ec47f6d75
Source noteuspto-grants-2009_01