HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049911Generated: November 1, 2026
Isopropyl iodide → 6-(3-fluorophenyl)-N-isopropylpyrido[3,2-d]pyrimidin-4-amine
https://huagongshe.com/reaction/1049911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-(3-Fluorophenyl)pyrido[3,2-d]pyrimidin-4-amine | HCID 86703914 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(3-fluorophenyl)-N-isopropylpyrido[3,2-d]pyrimidin-4-amine | HCID 86703913 | — |
Reaction Steps
6-(3-fluorophenyl)pyrido[3,2-d]pyrimidin-4-amine 1 (100 mg, 0.42 mmol) in DMF was treated with sodium hydride 60% dispersion in mineral oil (25 mg, 0.63 mmol) followed by 2-iodopropane (0.04 mL, 0.42 mmol), stirred at room temperature for 2 hrs. The reaction mixture was poured on ice, and extracted with EtOAc three times. The combined organic layers were dried with sodium sulfate and concentrated to dry. The crude was purified by ISCO eluting with 100% EtOAc to give pure 6-(3-fluorophenyl)-N-isopropylpyrido[3,2-d]pyrimidin-4-amine 25. LC/MS (ESI+): m/z 283 (M+H). 1H NMR (400 MHz, DMSO) δ 8.53-8.43 (m, 2H), 8.37 (d, J=10.8 Hz, 1H), 8.21 (t, J=8.4 Hz, 2H), 8.15 (d, J=8.8 Hz, 1H), 7.60 (dd, J=14.2, 8.0 Hz, 1H), 7.34 (td, J=8.5, 2.5 Hz, 1H), 4.56 (dq, J=13.3, 6.7 Hz, 1H), 1.35 (d, J=6.6 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382241B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-6a5b85cf8d1a4fa285e3dca673f85b70 |
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| Source note | uspto-grants-2016_07 |
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