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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991560Generated: November 2, 2026

Dichloromethane → HCID 73443602, compound

https://huagongshe.com/reaction/991560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 131723544HCID 131723544—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 73443602HCID 73443602—

Reaction Steps

Tetrakis(triphenylphosphine)palladium (O) (10 mol %, 58 mg) was added to a mixture of the compound of Example 13, Isomer A (288 mg, 0.493 mmol) and phenyl boronic acid (90 mg, 0.74 mmol) in DME (10 ml) and sodium carbonate (2M, 0.986 mmol, 0.493 ml). The mixture was heated at 80° overnight, dlute with CH2Cl2 (200 ml), washed with diluted HCl and sodium hydrogen carbonate solution, dried (Na2SO4) and evaporated in vacuo. Chromatography (SiO2; CH2Cl2/MeOH, 93:7) gave the title compound as a white solid (133 mg). δH (DMSO-d6), 11.04 (1H, s, CONH), 10.40 (1H, s, CONH), 8.79 (2H, s, Cl2PyH), 8.48 (1H, dd, J 4.9, 1.9 Hz, PyH), 7.85 (1H, dd, J 7.5, 1.9 Hz, PyH), 7.66 (2H, d, J 8.7 Hz, ArH), 7.51 (1H, dd, J 7.5, 4.9 Hz, PyH), 7.39-7.35 (3H, m, ArH), 7.23 (2H, d, J 8.7 Hz, ArH), 7.07 (2H, m, ArH) and 3.45 (3H, s, CO2Me); m/z (ESI, 60V) 581 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465471B1
Source datasetuspto-grants-2002_10
ORD IDord-3c85a4aa060d42b0a2fff181d5b7d1fa
Source noteuspto-grants-2002_10