HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279732Generated: October 30, 2026
Diisopropylethylamine → 2-amino-5-bromo-4-fluoro-N-methylbenzamide
https://huagongshe.com/reaction/2279732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 2-Amino-5-bromo-4-fluoro-benzoic acid | HCID 28827257 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-amino-5-bromo-4-fluoro-N-methylbenzamide | HCID 86697689 | — |
Reaction Steps
A solution of 2-amino-5-bromo-4-fluorobenzoic acid (2.00 g, 8.55 mmol), methylamine hydrochloride (0.692 g, 10.2 mmol), TBTU (2.74 g, 8.55 mmol), and DIPEA (4.46 mL, 25.6 mmol) in DCM (15.0 mL) was stirred at rt for 30 minutes. The reaction was quenched with sat. aq. NaHCO3 (10 mL) and extracted with DCM (15 mL). The organic layer was washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to a yellow oil. The crude material was purified on a Teledyne ISCO Combiflash® Rf system using DCM/MeOH (100:0→95:5) as eluent to afford the title compound as 2.54 g of a white solid. 1H NMR (CDCl3, 400 MHz): δ 7.48 (d, J=7.3 Hz, 1H), 6.44 (d, J=10.4 Hz, 1H), 6.11 (br. s., 1H), 5.66 (br. s., 2H), 2.96 (d, J=4.8 Hz, 3H). MS (ESI): m/z 248.91 [M+H]+. UPLC: tR=3.26 min (ZQ3: polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09133224B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-a841954fd94f4183b3e2da80597d9995 |
|---|
| Source note | uspto-grants-2015_09 |
|---|