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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416186Generated: November 2, 2026

1,2-Dichloroethane → HCID 86610489, compound

https://huagongshe.com/reaction/2416186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant2-AminobenzaldehydeHCID 68255—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
ReactantHCID 86610488HCID 86610488—
SolventDichloromethaneHCID 6344—
ProductHCID 86610489HCID 86610489—

Reaction Conditions

Temperature0 °C

Reaction Steps

In an oven-dried, 50-mL, round-bottomed flask were placed 2-(4-pyridyl)-thiazole acetic acid (Step b, 140 mg, 0.64 mmol), 2-aminobenzaldehyde (Aldrich, 270 mg, 2.22 mmol), EDC (Aldrich, 244 mg, 1.27 mmol), and DIEA (Aldrich, 148 mg, 0.20 mL, 1.15 mmol) in CH2Cl2 (20 mL). The mixture was cooled to 0° C., and 1-hydroxy-7-azabenzotriazole (Aldrich, 173 mg, 1.27 mmol) was added in one portion. The reaction was warmed to RT slowly, stirred for 12 h, and concentrated in vacuo. The resulting crude product was purified by flash chromatography (EtOAc/hexanes, 50:50) to afford N-(2-formylphenyl)-2-(4-pyridyl)-thiazole acetamide as a white solid. Mp: 136-137° C. MS m/z: 324 (M+1). Calc'd for C17H13N3O2S: 323.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822097B1
Source datasetuspto-grants-2004_11
ORD IDord-1801a2ac7d7d4118a93e47213a7f23fe
Source noteuspto-grants-2004_11