HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284764Generated: October 31, 2026
Phosphorus oxychloride → 4-((4-Chloro-5-iodopyrimidin-2-yl)amino)benzonitrile
https://huagongshe.com/reaction/2284764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178513662 | HCID 178513662 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-((4-Chloro-5-iodopyrimidin-2-yl)amino)benzonitrile | HCID 90051782 | — |
Reaction Steps
To 4-((4-hydroxy-5-iodopyrimidin-2-yl)amino)benzamide (J11, 1.35 g), phosphorus oxychloride (14 mL) was added at room temperature, and the mixture was stirred at 90° C. for 1 hour and 30 minutes. The reaction mixture was cooled to room temperature, and then poured into ice, and then ethyl acetate was added to the mixture. The organic layer was separated, washed successively with water, saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained solid matter was washed with a mixed solvent of diisopropyl ether and chloroform, and then dried under reduced pressure to obtain 4-((4-chloro-5-iodopyrimidin-2-yl)amino)benzonitrile (J12, 764 mg) as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145415B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-fca696d3241647fa8174938fe8d92496 |
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| Source note | uspto-grants-2015_09 |
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