HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914877Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 67253227, compound
https://huagongshe.com/reaction/1914877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 68313323 | HCID 68313323 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl orthoformate | HCID 31214 | — |
| Product | HCID 67253227 | HCID 67253227 | 535.3% |
Reaction Steps
A mixture of 5-amino-6,7-difluoro-1-(2-fluoro-4-iodo-phenyl)-4-hydroxy-1,3-dihydro-benzoimidazol-2-one (I-13a: 550 mg, 1.3 mmol) in triethyl orthoformate (5 mL) and p-toluene sulfonic acid (20 mg, 0.13 mmol) were taken in a flask and the flask was heated to reflux at 120° C. for 30 minutes. The reaction was monitored by TLC (70% ethyl acetate in hexane). The reaction mixture was concentrated under reduced pressure and the concentrate was triturated with diethyl ether and filtered. The residue was washed with diethyl ether and dried under reduced pressure to afford 300 mg of the product (54.5% yield). H1NMR (DMSO-d6, 300 MHz): δ 12.50 (s, 1H), 8.87 (s, 1H), 7.97 (dd, 1H), 7.78 (d, 1H), 7.50 (t, 1H). LCMS: 92.2%, m/z=431.9 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08614239B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-66c732bbf0ae4818aeb2a84d6907bf44 |
|---|
| Source note | uspto-grants-2013_12 |
|---|