HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188987Generated: October 29, 2026
Trifluoroacetic acid → 4-(2-(4-Cyanophenylamino)thieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile
https://huagongshe.com/reaction/2188987
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | 4-(2-Chlorothieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile | HCID 57848878 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-(4-Cyanophenylamino)thieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile | HCID 24795081 | 14.5% |
Reaction Steps
To a solution of 4-(2-chlorothieno[2,3-d]pyrimidin-4-yloxy)-3,5-dimethylbenzonitrile (188 mg, 0.59 mmol), TFA (0.37 mL, 4.75 mmol) in TFE (2.5 mL) was added 4-aminobenzonitrile (280 mg, 2.37 mmol) in a sealed tube. The reaction was stirred at 90° C. for 2 d. Reaction mixture was diluted with ethyl acetate (5 mL) and washed with saturated NaHCO3 (3×10 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by HPLC afforded the product as white solid (34 mg, 14%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324223B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-929239d62ae042dbb487f9c30ed98b1e |
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| Source note | uspto-grants-2012_12 |
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