HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → HCID 67173846, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| 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 67173846 | HCID 67173846 | 52.9% |
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 CbzCl (151 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 %: 15%-40%, 25 min) to give the title compound (220 mg, 42%) as TFA salt. 1H NMR: DMSO 400 MHz δ 9.97 (s, 1H), 7.63 (t, J=7.2 Hz, 1H), 7.55 (q, 1H), 7.42 (q, 1H), 7.37 (q, 3H), 7.32 (q, 3H), 7.30 (q, 3H), 6.52 (s, 1H), 6.37 (q, 1H), 5.05 (s, 2H), 4.83 (s, 2H), 4.53 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461134B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-0e5c06a5b1de4d4f9849a979fa5a29ad |
| Source note | uspto-grants-2013_06 |