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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441434Generated: November 1, 2026

5-Indolylboronic acid → HCID 11472679, compound

https://huagongshe.com/reaction/1441434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Indolylboronic acidHCID 2734361—
ReactantHCID 86598854HCID 86598854—
ProductHCID 11472679HCID 11472679—

Reaction Steps

The product of Example 30A (270 mg, 1.1 mmol) was coupled with 5-indolylboronic acid (215 mg, 1.4 mmol) according to the procedure of Example 20B. The title compound was purified by preparative HPLC (Xterra™, column, Xterra RP-18 5 μm, 30×100 mm. Eluting Solvent, MeCN/H2O (NH4HCO3, 0.1 M, PH=10) (v. 90/10 to 10/90 over 20 min.) Flow rate, 75 mL/min., uv, 250 nm) as solid (200 mg, 57%). 1H NMR (300 MHz, MeOH-D4) δ 1.49-1.63 (m, 1H), 1.67-1.92 (m, 2H), 1.99-2.14 (m, 1H), 2.28-2.36 (m, 1H), 2.76-3.04 (m, 5H), 3.48 (ddd, J=14.7, 8.2, 1.9 Hz, 1H), 5.24-5.34 (m, 1H), 6.56 (d, J=4.1 Hz, 1H), 7.24 (d, J=9.5 Hz, 1H), 7.30 (d, J=3.4 Hz, 1H), 7.50 (d, J=8.5 Hz, 1H), 7.73 (dd, J=8.6, 1.9 Hz, 1H), 8.07 (d, J=9.5 Hz, 1H), 8.13 (s, 1H) ppm. MS (DCI/NH3) m/z 321 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655657B2
Source datasetuspto-grants-2010_02
ORD IDord-ea68b4b16e89485ab813e16d47a56e8d
Source noteuspto-grants-2010_02