HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570963Generated: November 1, 2026
Triphenylphosphine Oxide → HCID 135985851, compound
https://huagongshe.com/reaction/570963
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine Oxide | HCID 13097 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | HCID 66831845 | HCID 66831845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 135985851 | HCID 135985851 | 56.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09024018B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-fe2a04e7b04f4a3597d795e6e3b13c59 |
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| Source note | uspto-grants-2015_05 |
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