HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50820Generated: October 28, 2026
3-Bromoaniline → N-(3-bromophenyl)pyrido[3,4-d]pyrimidin-4-amine
https://huagongshe.com/reaction/50820
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | 4-Methylthiopyrido[3,4-d]pyrimidine | HCID 23240465 | — |
| Product | N-(3-bromophenyl)pyrido[3,4-d]pyrimidin-4-amine | HCID 5328257 | 52.7% |
Reaction Steps
A mixture of 4-methylthiopyrido[3,4-d]pyrimidine (75 mg, 0.42 mmol) (see previous experimental), and 3-bromoaniline (1 mL) is heated to 10° C. under N2 for 2 h. The reaction mixture is then chromatographed on silica using MPLC and eluting with a gradient system (CHCl3 to 5% MeOH in CHCl3). The fractions are concentrated under reduced pressure, and the resulting solid is recrystallized from Et2O to yield 4-(3-bromoanilino)pyrido[3,4-d]pyrimidine (66 mg, 52.7%) as a light brown solid. 1H NMR (DMSO) δ 10.15 (1H, s), 9.21 (1H, s), 8.80 (1H, s), 8.76 (1H, d, J=5.8 Hz), 8.44 (1H, d, J=5.6 Hz), 8.25 (1H, s), 7.93 (1H, d, J=7.7 Hz), 7.45-7.37 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713484B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-e47552f259f0432bba4aee43fc64e471 |
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| Source note | uspto-grants-2004_03 |
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