HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928952Generated: October 30, 2026
Trifluoroacetic acid → HCID 89704789, compound
https://huagongshe.com/reaction/928952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 89704884 | HCID 89704884 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 89704789 | HCID 89704789 | 61.2% |
Reaction Steps
To a solution of 4-fluoro-5-((2-fluorophenyl)amino)benzo[d]oxazole-6-carboxylic acid (7.22 g, 24.88 mmol) in DMF (50 mL) was added NIS (6.08 g, 26.37 mmol) followed by trifluoroacetic acid (1.0 mL). After stirring for 5 h at ambient temperature, the reaction was quenched by saturated NH4Cl (aq.). The solution was extracted with ethyl acetate (150 mL×3). The combined organic extracts were washed with water (100 mL) and brine (100 mL) successively, dried over Na2SO4 and concentrated in vacuo. The crude product was purified by column chromatography on silica gel (CH2Cl2/MeOH, 50:1, v/v) and gave the desired product (brown solid, 6.34 g, 61.2% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.97 (s, 1H), 8.58 (s, 1H), 8.18 (s, 1H), 7.58 (dd, J=11.0, 1.7 Hz, 1H), 7.34 (d, J=8.5 Hz, 1H), 6.55 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09290468B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-b5923e90dd5141f788f342b9f2cb6672 |
|---|
| Source note | uspto-grants-2016_03 |
|---|