Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306600Generated: November 2, 2026

(Iodomethyl)cyclopentane → HCID 22609911, compound

https://huagongshe.com/reaction/2306600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Iodomethyl)cyclopentaneHCID 2762531—
ReactantHCID 22609889HCID 22609889—
ProductHCID 22609911HCID 22609911—

Reaction Steps

This compound was prepared using the procedure described in Example 27 Step c) with cyclopentylmethyl iodide used instead of neopentyl iodide and 3-(2-fluorophenyl)-7-iodo-6-(2-methyl-2H-1,2,4-triazol-3-ylmethoxy)-1,2,4-triazolo[4,3-b]pyridazine used instead of 7-bromo-3-(2-fluorophenyl)-6-(2-methyl-2H-1,2,4-triazol-3-ylmethoxy)-1,2,4-triazolo[4,3-b]pyridazine. Data for the title compound: m.p. 135-137° C.; 1H NMR (360 MHz, CDCl3) δ 1.18-1.28 (2H, m), 1.36-1.74 (4H, m), 1.76-1.86 (2H, m), 2.16-2.28 (1H, m), 2.66 (2H, d, J=7 Hz), 3.84 (3H, s), 5.49 (2H, s), 7.25-7.30 (1H, m), 7.36 (1H, dd, J=7 and 7 Hz), 7.50-7.60 (1H, m), 7.82-7.86 (2H, m), 7.89 (1H, s); MS (ES+) m/e 382 [MH]+. Anal. Found C, 60.85; H, 5.38%. C21H22FN7O.0.4H2O requires C, 60.83; H, 5.54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828322B2
Source datasetuspto-grants-2004_12
ORD IDord-e4aa28de2cca4adb8929ad1e07df6e2e
Source noteuspto-grants-2004_12