HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50792Generated: October 25, 2026
2-Bromoaniline → 4-N-(2-bromophenyl)pyrido[4,3-d]pyrimidine-4,7-diamine
https://huagongshe.com/reaction/50792
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoaniline | HCID 11992 | — |
| Reactant | 7-Amino-4-methylthiopyrido[4,3-d]pyrimidine | HCID 10442562 | — |
| Product | 4-N-(2-bromophenyl)pyrido[4,3-d]pyrimidine-4,7-diamine | HCID 5328055 | 33.2% |
Reaction Steps
A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (198 mg, 1.03 mmol) (described in a previous experimental) and 2-bromoaniline (1.00 mL, 9.18 mmol) is stirred under N2 at 180° C. for 2.5 h, and the resulting product is chromatographed on alumina (1% EtOH/CHCl3) to give 7-amino-4-(2-bromoanilino)pyrido[4,3-d]pyrimidine (108 mg, 33%) as a pale yellow solid, 1H NMR (DMSO) δ 9.91 (1H, brs), 9.27 (1H, s), 8.20 (1H, s), 7.73 (1H, d, J=7.9 Hz), 7.50 (1H, m), 7.44 (1H, t, J=6.9 Hz), 7.25 (1H, m), 6.59 (2H, brs), 6.42 (1H, s).
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-7aabd9d42fcc4be08d55aaaaf2ebeace |
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| Source note | uspto-grants-2004_03 |
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