Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Benzylhydroxylamine | HCID 102313 | — |
| Reactant | HCID 86663797 | HCID 86663797 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 49869277 | HCID 49869277 | 72% |
Reaction Steps
4-oxo-3-(prop-2-ynyl)-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylic acid (0.46 mmol, 100 mg, 1 eq.), O-Benzotriazole-N,N,N′,N′-tetramethyl-uronium-hexafluoro-phosphate (HBTU) (0.55 mmol, 208 mg, 1.2 eq.) and triethylamine (0.55 mmol, 77 μL, 1.2 eq.) were dissolved in THF (30 mL) and DMF (1 mL). The mixture was stirred at room temperature for 1 hour before adding O-benzylhydroxylamine (0.55 mmol, 68 mg, 1.2 eq.) in one portion. After 24 hours of room temperature stirring, the volume of the solution was reduced to 5 mL and poured into ice/water. The formed solid was filtered and washed with water, ethyl acetate and ether, and dried under vacuum. Yield: 72%. δH (DMSO-d6) 11.93 (1H, bs), 8.89 (1H, s), 7.48 (2H, m), 7.40 (3H, m), 5.15 (2H, d, J: 1.84), 4.97 (2H, s), 3.53 (1H, bs).
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-bc3061ec4c594a2cbc45cb4d14afb154 |
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| Source note | uspto-grants-2015_05 |
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