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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764811Generated: November 2, 2026

Benzyl iodide → HCID 21302495, compound

https://huagongshe.com/reaction/1764811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl iodideHCID 12098—
Reactantethyl (10R,15S)-3-oxo-1,4,12-triazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16)-triene-12-carboxylateHCID 20578971—
ProductHCID 21302495HCID 21302495—

Reaction Steps

Utilizing the material from Example 255 Step A, the title compound was prepared in analogous fashion using benzyl iodide as the alkyl halide and following the procedure of Step B-D of Example 255, as a viscous liquid. 1H NMR (CDCl3, 300 MHz) δ 1.60-2.0 (m, 2H), 2.55-2.95(m, 4H), 2.95-3.15 (m, 2H), 3.20-3.45 (m, 3H), 4.40 (q, J=16.1 Hz, 2H), 6.41 (d, J=7.1 Hz, 1H), 6.51 (d, J=7.1 Hz, 1H), 6.62 (t, J=7.1 Hz, 1H), 7.20-7.40 (m, 5H) ppm. MS (CI): 306 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039680E1
Source datasetuspto-grants-2007_06
ORD IDord-96cfd72ec87b414b8227682ec6b53b4b
Source noteuspto-grants-2007_06