HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767685Generated: October 31, 2026
HCID 21114501, compound → HCID 58890823, compound
https://huagongshe.com/reaction/1767685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21114501 | HCID 21114501 | — |
| Reactant | HCID 22245024 | HCID 22245024 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58890823 | HCID 58890823 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235555B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-54f4f0bf442a47e1aa9a12f5c05d2092 |
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| Source note | uspto-grants-2007_06 |
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