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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantSodium hydrideHCID 24758—
Reactant6-(3-Fluorophenyl)pyrido[3,2-d]pyrimidin-4-amineHCID 86703914—
SolventDimethylformamideHCID 6228—
Product6-(3-fluorophenyl)-N-isopropylpyrido[3,2-d]pyrimidin-4-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382241B2
Source datasetuspto-grants-2016_07
ORD IDord-6a5b85cf8d1a4fa285e3dca673f85b70
Source noteuspto-grants-2016_07