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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473854Generated: November 2, 2026

Methyl iodide → HCID 59587980, compound

https://huagongshe.com/reaction/1473854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(4-(2H-tetrazol-5-yl)phenyl)-4-(3-morpholinophenyl)pyrimidin-2-amineHCID 59588150—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 59587980HCID 59587980—

Reaction Steps

A mixture of N-(4-(2H-tetrazol-5-yl)phenyl)-4-(3-morpholinophenyl)pyrimidin-2-amine (0.20 g, 0.50 mmol), MeI (0.71 g, 5.0 mmol) and K2CO3 (0.35 g, 2.50 mmol) in acetone (5 mL) was stirred at room temperature overnight. The reaction mixture was diluted with water, extracted with EtOAc (3×). The combined organic solution was dried over anhydrous MgSO4 and concentrated in vacuo to give a solid. Purification of this material by column chromatography on silica gel (40% EtOAc/hexane) provided N-(4-(2-methyl-2H-tetrazol-5-yl)phenyl)-4-(3 morpholinophenyl)pyrimidin-2-amine as the major product. 1H NMR (DMSO-d6, 400 MHz) δ 10.00 (s, 1H), 8.60 (d, 1H), 8.05 (d, 2H), 8.00 (d, 2H), 7.78 (s, 1H), 7.65 (d, 1H), 7.50 (d, 1H), 7.42 (t, 1H), 7.18 (dd, 1H), 4.42 (s, 3H), 3.80 (m, 4H), 3.24 (m, 4H). MS (ESI) 415.13 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018205B2
Source datasetuspto-grants-2015_04
ORD IDord-6b73848443fa404ea35df9936a82d43e
Source noteuspto-grants-2015_04