Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 20412-36-6 | HCID 13292916 | — |
| Reactant | 4-amino-2-(aminomethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)benzenesulfonamide | HCID 67173422 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67174238 | HCID 67174238 | 57.8% |
Reaction Steps
To a solution of 4-amino-2-(aminomethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)benzenesulfonamide (500 mg, 0.89 mmol) and TEA (360 mg, 3.6 mmol) in THF (200 mL) at −20° C. was slowly added 3-pentyl chloroformate (147 mg, 0.89 mmol) in THF (10 mL). Then the mixture was stirred at room temperature for 2 hrs. The mixture was concentrated in vacuo and the residue was purified by prep-HPLC (column: Luna 300×50.0 mm, 10 u; liquid phase: [A-H2O+0.025% TFA; B-MeCN] B %: 17%-42%, 25 min) to give the title compound (230 mg, 43%) as TFA salt. 1H NMR: DMSO 400 MHz δ 9.97 (s, 1H), 7.53 (d, J=8.4 Hz, 1H), 7.35 (q, 1H), 7.20 (d, J=8.4 Hz, 1H), 7.11 (J=8.4 Hz, 1H), 6.47 (s, 1H), 6.35 (q, 1H), 4.88 (s, 2H), 4.50 (q, 3H), 1.50 (q, 4H), 0.84 (t, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08461134B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-e7d0f4f98ae5445f9a57d8a35b6a8206 |
|---|
| Source note | uspto-grants-2013_06 |
|---|