HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11787Generated: October 25, 2026
Aniline → 3-(2,4-Diphenylamino-pyrimidin-5-yl)-2-pyridin-3-yl-propionic acid ethyl ester
https://huagongshe.com/reaction/11787
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aniline | HCID 6115 | — |
| Reactant | 3-(2,4-Dichloro-pyrimidin-5-yl)-2-pyridin-3-yl-propionic acid ethyl ester | HCID 21044303 | — |
| Product | 3-(2,4-Diphenylamino-pyrimidin-5-yl)-2-pyridin-3-yl-propionic acid ethyl ester | HCID 21044307 | — |
Reaction Steps
A mixture of 3-(2,4-dichloro-pyrimidin-5-yl)-2-pyridin-3-yl-propionic acid ethyl ester (326 mg, 1.0 mmol) (from Example 10a supra) and aniline (2.0 mL) (Aldrich) was heated at 120° C. for 1 hour. The reaction mixture was washed with hexanes (50 mL×3) and the supernatant was decanted off after each time. The residue was then dissolved in ethyl acetate (100 mL) and successively washed with saturated aqueous ammonium chloride solution (30 mL), water (30 mL) and brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude product was purified by preparative thin layer chromatography to give 3-(2,4-diphenylamino-pyrimidin-5-yl)-2-pyridin-3-yl-propionic acid ethyl ester as a brown solid which was used in the next step without further purification. (Yield 60 mg, 13.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098332B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-574db29389fe441fb2573534e99b8d0c |
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| Source note | uspto-grants-2006_08 |
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