HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50784Generated: October 25, 2026
3-Aminophenol → 3-({7-Aminopyrido[4,3-d]pyrimidin-4-yl}amino)phenol
https://huagongshe.com/reaction/50784
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | 7-Amino-4-methylthiopyrido[4,3-d]pyrimidine | HCID 10442562 | — |
| Product | 3-({7-Aminopyrido[4,3-d]pyrimidin-4-yl}amino)phenol | HCID 5328072 | 27.3% |
Reaction Steps
A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (299 mg, 1.56 mmole) and 3-aminophenol (1.60 g, 14.7 mmole) is stirred at 160° C. for 15 min. The resulting product is chromatographed over silica gel (9% MeOH/CH2Cl2) to give 7-amino-4-(3-hydroxyanilino)pyrido[4,3-d]pyrimidine (108 mg, 18%) as a pale orange solid. 1H NMR (DMSO) δ 9.69 (1H, brs), 9.44 (1H, brs), 9.33 (1H, s), 8.38 (1H, s), 7.37 (1H, t, J=2.1 Hz), 7.21 (1H, brd, J=8.4 Hz), 7.14 (1H, t, J=8.0 Hz), 6.59 (2H, brs), 6.53 (1H, ddd, J=7.9, 2.2, 0.8 Hz), 6.43 (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-9df614f5da23401fa07263347eb122d1 |
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| Source note | uspto-grants-2004_03 |
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