HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 4-Fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 3-Amino-4-fluorobenzoic acid | HCID 75396 | — |
| Reactant | 2-(Pyridin-2-ylamino)thiazole-5-carbaldehyde | HCID 22019058 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid | HCID 22019056 | 91.3% |
Reaction Steps
To a suspension of 2-(pyridin-2-ylamino)-thiazole-5-carbaldehyde (1.0 g, 4.90 mmol, compound 1A) in methylene chloride (20 mL) at RT 3-amino-4-fluorobenzoic acid (0.95 g, 4.90 mmol) TFA (5 mL) and triethylsilane (1.71 mg, 14.7 mmol) were added. The above reaction mixture was stirred at RT for 4 h, then concentrated in vacuo and the resulting slurry was triturated with methanol to afford 4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid as light yellow solid (1.54 g, 91%) (M+H)+=345.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547711B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-9feb685a2c5e4825859ad868702b2ffd |
| Source note | uspto-grants-2009_06 |