HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256129Generated: October 30, 2026
Triethylamine → 2-(5-Amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)-N-(prop-2-ynyl)acetamide
https://huagongshe.com/reaction/1256129
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propargylamine | HCID 239041 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 53234452 | HCID 53234452 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(5-Amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)-N-(prop-2-ynyl)acetamide | HCID 86655218 | — |
Reaction Steps
To the mixture of 2-(5-amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetic acid (363 mg, 1 mmol) and propargyl amine (0.2 ml, 3 mmol) in DMF (5 ml), added PyBOP (520 mg, 1 mmol) then triethyl amine (0.3 ml, 2 mmol). Stirring was kept for 3 hours. Diluted with EtOAc, washed with 1N HCl, water and brine. Dried over anhydrous sodium sulfate. Concentrated, the residue was dissolved in DMSO and purified by prep HPLC (SunFire Prep C18 OBD 5 uM 30×50 mm column). The title compound was obtained as white powder. MS calcd for (C18H18BN3O5S): 399.11. MS found (ESI negative): (M−H)−=398.03. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.80 (s, 1H), 9.1 (br, 1H), 8.42 (t, J=4.8 Hz, 1H), 7.44 (s, 1H), 7.43 (d, J=8.4 Hz, 1H), 7.22 (d, J=8 Hz, 1H), 7.13 (dd, J=8.4 Hz, 1H), 6.44 (d, J=2 Hz, 1H), 6.36 (dd, J=8.8 Hz, 1H), 4.87 (s, 2H), 3.91 (m, 2H), 3.80 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461134B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-53da7ecd194343bd8675299f4dfaf1a4 |
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| Source note | uspto-grants-2013_06 |
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