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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267053Generated: November 2, 2026

Benzyl iodide → HCID 21302495, compound

https://huagongshe.com/reaction/1267053

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 numberUS06552017B1
Source datasetuspto-grants-2003_04
ORD IDord-bb6966aa9bb54dd39c44154707d8190f
Source noteuspto-grants-2003_04