HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482875Generated: October 30, 2026
Pivalic acid → N-(3-bromo-5-methylphenyl)-4-cyclopropyl-2-pyrimidinamine
https://huagongshe.com/reaction/1482875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | 3-Bromo-5-methylaniline | HCID 3018526 | — |
| Reactant | 2-Chloro-4-cyclopropylpyrimidine | HCID 24901915 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(3-bromo-5-methylphenyl)-4-cyclopropyl-2-pyrimidinamine | HCID 118103319 | — |
Reaction Steps
To a solution of 2-chloro-4-cyclopropyl-pyrimidine (12.5 g, 81 mmol) and 3-bromo-5-methylaniline (18.1 g, 97 mmol) in 1,4-dioxane (100 mL) was added pivalic acid (9.3 mL, 81 mmol). The resulting mixture was heated to reflux and left stirring for 10 hours. The mixture was allowed to cool to room temperature and hexanes were added (80 mL). The slurry was filtered and the filtrate was washed with MeOH to afford a portion of N-(3-bromo-5-methylphenyl)-4-cyclopropylpyrimidin-2-amine. The mother liquors were concentrated, absorbed on silica gel and purified by silica gel column chromatography (EtOAc/Hex) to afford additional N-(3-bromo-5-methylphenyl)-4-cyclopropylpyrimidin-2-amine as a white solid. MS ESI calcd. for C14H15BrN3 [M+H]+ 304 and 306. found 304 and 306.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416111B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-d7b7b2125f544977bfc860628a301285 |
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| Source note | uspto-grants-2016_08 |
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