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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245612Generated: November 2, 2026

Methyl iodide → HCID 21912762, compound

https://huagongshe.com/reaction/1245612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantIodoethaneHCID 6340—
ReactantHCID 21912742HCID 21912742—
ReactantHCID 21912822HCID 21912822—
ProductHCID 21912762HCID 21912762—

Reaction Steps

The title compound was prepared from 1-(tert-butoxycarbonyl)-4-(1-ethyl-3-hydroxymethyl-4-methyl-(1H)-pyrazol-5-yl)piperidine (from Piperidine 19, Step C) using a procedure analogous to that described for Piperidine 15, Step E, except methyliodide was substutited for ethyliodide. RF: 0.47 (3:2 v/v hexanes/acetone); 1H-NMR (500 MHz) δ 1.39 (t, J=7.2, 3H), 1.49 (s, 9H), 1.69–1.71 (m, 2H), 1.85–1.94 (m, 2H), 2.08 (s, 3H), 2.75–2.81 (m, 3H), 3.39 (s, 3H), 4.12 (q, J=7.2, 2H), 4.14–4.27 (m, 2H), 4.38 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125887B2
Source datasetuspto-grants-2006_10
ORD IDord-85555e29019a4a71850fd9a637f57ee4
Source noteuspto-grants-2006_10