HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416186Generated: November 2, 2026
1,2-Dichloroethane → HCID 86610489, compound
https://huagongshe.com/reaction/2416186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 2-Aminobenzaldehyde | HCID 68255 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | HCID 86610488 | HCID 86610488 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86610489 | HCID 86610489 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06822097B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-1801a2ac7d7d4118a93e47213a7f23fe |
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| Source note | uspto-grants-2004_11 |
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