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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767685Generated: October 31, 2026

HCID 21114501, compound → HCID 58890823, compound

https://huagongshe.com/reaction/1767685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21114501HCID 21114501—
ReactantHCID 22245024HCID 22245024—
ReactantHCID 178418922HCID 178418922—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58890823HCID 58890823—

Reaction Conditions

Temperature35 °C

Reaction Steps

2-[2-Chloro-3-methyl-5-(4-methyl-piperazin-1-yl)-phenyl]-acetamide (211 mg, 0.75 mmol) and 3-indoleglyoxylate (270 mg, 1.35 mmol) are dissolved in THF (5 mL). A solution of 1.0 M tert-BuOK in THF (2.98 mL, 4 eq) is added and the mixture is stirred at 35° C. overnight. The reaction is diluted with AcOEt (20 mL) and washed with H2O (20 mL) and brine (10 mL). The organic phase is dried over Na2SO4 and the solvent is evaporated. The residue is purified by FCC (AcOEt/AcOH/H2O 7:1:1) to afford the title compound in the form of its acetate salt. 1H NMR (DMSO, 400 MHz) δ 2.16 (s, 3H), 2.31 (s, 3H), 2.32-2.38 (m, 4H), 2.97-3.10(m, 4H), 6.61 (d, J=8.0 Hz, 1H), 6.71-6.77 (m, 2H), 7.04 (d, J=2.8 Hz, 1H), 7.08(dd,J=7.4, 7.2 Hz, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.98 (d, J=1.5Hz, 1H), 11.05 (br s, 1H), 11.90(br s, 1H); ES-MS: 435 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235555B2
Source datasetuspto-grants-2007_06
ORD IDord-54f4f0bf442a47e1aa9a12f5c05d2092
Source noteuspto-grants-2007_06