HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256130Generated: October 30, 2026
Benzylamine → 2-(5-Amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)-N-benzylacetamide
https://huagongshe.com/reaction/1256130
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| 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-benzylacetamide | HCID 53234535 | — |
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 (500 mg, 1.4 mmol) and benzyl amine (0.5 ml, 4.5 mmol) in DMF (5 ml), added PyBOP (730 mg, 1.4 mmol) then triethyl amine (0.4 ml, 3 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 (C22H22BN3O5S): 451.14. MS found (ESI negative): (M−H)−=450.1. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.78 (s, 1H), 9.15 (br, 1H), 8.38 (t, J=6 Hz, 1H), 7.37 (d, J=1.2 Hz, 1H), 7.36 (d, J=8.8 Hz, 1H), 7.30-7.10 (m, 6H), 7.01 (dd, J=8.4 Hz, 1H), 6.43 (d, J=2 Hz, 1H), 6.30 (dd, J=8.4 Hz, 1H), 4.80 (s, 2H), 4.25 (d, J=5.6 Hz, 1H), 3.79 (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-fea7c246b3414f73a00badca01a76729 |
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| Source note | uspto-grants-2013_06 |
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