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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570963Generated: November 1, 2026

Triphenylphosphine Oxide → HCID 135985851, compound

https://huagongshe.com/reaction/570963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphine OxideHCID 13097—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 66831845HCID 66831845—
SolventDichloromethaneHCID 6344—
ProductHCID 135985851HCID 13598585156.2%

Reaction Steps

Triflic anhydride (820 μL; 4.85 mmol) was added to a solution of triphenylphosphine oxide (1.35 g; 4.85 mmol) in DCM (15 mL) at 0° C. and the mixture stirred for 20 minutes, then added to a suspension of N-(2-aminophenyl)-3-(methoxymethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide (0.500 g; 1.61 mmol—combined batches) in DCM (15 mL). The solution was stirred for 96 hours, and the precipitate filtered. This was the triflate salt of the desired product (550 mg). This salt was dissolved in a mixture of MeCN (19 mL) and MeOH (1 mL) and triethylamine (750 μL) added. The resulting precipitate was filtered, and washed with ethyl acetate to give the title compound as a yellow powder (269 mg; 56%). Concentration of the filtrate, and washing the residue with ethyl acetate yielded a further 48 mg of pure material. δH (DMSO d6): 13.09 (1H, s), 7.75 (1H, d, J=7.5), 7.58 (1H, d, J=7.1), 7.30-7.22 (2H, m), 5.64 (2H, s), 3.45 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024018B2
Source datasetuspto-grants-2015_05
ORD IDord-fe2a04e7b04f4a3597d795e6e3b13c59
Source noteuspto-grants-2015_05