HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987547Generated: October 25, 2026
2-Bromo-4-methylaniline → 4-(4-Hydroxyanilino)-6-(2-bromo-4-methylanilino)pyrimidine
https://huagongshe.com/reaction/987547
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromo-4-methylaniline | HCID 11422 | — |
| Reactant | 4-(4-Hydroxyanilino)-6-chloropyrimidine | HCID 18009128 | — |
| Product | 4-(4-Hydroxyanilino)-6-(2-bromo-4-methylanilino)pyrimidine | HCID 18009141 | 4% |
Reaction Steps
To a solution of 4-(4-hydroxyanilino)-6-chloropyrimidine (Reference Example 5, 5 g) was added 2-bromo-4-methylaniline (7.5 ml) and the reaction mixture was heated at 195° C. for 24 hours. The residue was absorbed onto silica and purified by column chromatography eluting with DCM:MeOH (19:1) to give the title compound (336 mg, 4%). NMR: 2.28 (3H, s), 5.72 (1H, s), 6.68 (2H, d), 7.17 (3H, m), 7.39 (1H, d), 7.48 (1H, s), 8.05 (1H, s), 8.38 (1H, s), 8.65 (1H, s), 9.08 (1H, s); m/z 371 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06632820B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-2cd86b8785844026bd2ff6d6d8213924 |
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| Source note | uspto-grants-2003_10 |
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