HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875252Generated: November 1, 2026
1,2-Dichloroethane → HCID 178509907, compound
https://huagongshe.com/reaction/1875252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 3-{[3-(Aminomethyl)-6-bromo-2-fluorophenyl]oxy}-5-chlorobenzonitrile | HCID 67197166 | — |
| Reactant | 4-chloro-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-5-carboxylic acid | HCID 68485533 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178509907 | HCID 178509907 | 2.8% |
Reaction Steps
EDC (0.028 g, 0.148 mmol) and HOBT (0.020 g, 0.148 mmol) were added to a solution of 3-{[3-(aminomethyl)-6-bromo-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.053 g, 0.148 mmol) and 4-chloro-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-5-carboxylic acid (0.041 g, 0.148 mmol) in DMF (2 mL). The mixture was stirred at RT overnight. The reaction mixture was extracted with ethyl acetate and saturated aqueous sodium bicarbonate. The organic layer was dried over sodium sulfate and concentrated to give a yellow oil which was dissolved in dichloromethane (1.5 mL). Trifluoroacetic acid (0.5 ml, 6.49 mmol) was added and the mixture was stirred at RT overnight. Purification by reverse phase HPLC (acetonitrile:water with 0.1% formic acid) gave the title compound 0.002 g, 2.5%) as a white solid. 1H NMR (400 MHz, methanol-d4) δ ppm 7.69 (s, 1H), 7.48-7.55 (m, 2H), 7.29 (t, 1H), 7.22 (d, 1H), 7.19 (s, 1H), 4.61 (s, 2H). ES MS m/z 483 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-fa3e649daf8c463f8b9a2ed5812e1a80 |
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| Source note | uspto-grants-2012_11 |
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