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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789967Generated: October 29, 2026

Benzyl iodide → HCID 21302495, compound

https://huagongshe.com/reaction/1789967

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 numberUS07071186B2
Source datasetuspto-grants-2006_07
ORD IDord-613b4223845d4184ab9b9410adf77fb2
Source noteuspto-grants-2006_07