HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422652Generated: October 29, 2026
1,2-Dichloroethane → HCID 53629051, compound
https://huagongshe.com/reaction/422652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Cyclobutanecarboxylic acid | HCID 19494 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 86608527 | HCID 86608527 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53629051 | HCID 53629051 | — |
Reaction Steps
(3-Chloropyrazin-2-yl)(3-phenylquinoxalin-6-yl)methyl-amine (106 mg, 0.30 mmol) and cyclobutanecarboxylic acid (51 mg, 0.46 mmol) were dissolved in DCM (10 mL). EDC (93 mg, 0.49 mmol) and HOBt hydrate (62 mg, 0.46 mmol) were added in sequence followed by N,N-diisopropylethylamine (0.15 mL, 0.83 mmol). The reaction was stirred at rt under Ar for 24 h then evaporated to dryness and purified by flash chromatography (0-1.5% MeOH in DCM) to afford a reddish oil. The material was dissolved in DCM (50 mL), washed with satd NaHCO3 (2×), H2O (1×), brine (1×), dried (MgSO4) and concentrated under reduced pressure (light yellow oil). Purification by flash chromatography (silica gel, 33% to 65% EtOAc in hexanes) afforded the title compound as a white solid; 1H NMR (400 MHz, CD3CN) δ 9.40 (s, 1H), 8.60 (d, J=2.8 Hz, 1H), 8.39 (d, J=2.4 Hz, 1H), 8.30-8.25 (m, 2H), 8.06 (d, J=8.4 Hz, 1H), 8.02 (s, 1H), 7.80 (dd, J=2.0 Hz, 8.8 Hz, 1H), 7.85-7.75 (m, 3H), 7.51 (d, J=7.8 Hz, 1H), 6.77 (d, J=8.0 Hz, 1H), 3.20 (quintet, J=8.4 Hz, 1H), 2.25-2.05 (m, 4H), 1.85-1.75 (m, 2H).). MS (ES+): m/z 430.0 (100) [MH+]; HPLC: tR=3.40 min (OpenLynx, polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101613B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-39e17baad7a645bf817a1b0e3531a159 |
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| Source note | uspto-grants-2012_01 |
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