HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012161Generated: October 25, 2026
1,2-Dichloroethane → HCID 178522446, compound
https://huagongshe.com/reaction/1012161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 6-Chloropyridine-3,4-diamine | HCID 817133 | — |
| Reactant | HCID 178524951 | HCID 178524951 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178522446 | HCID 178522446 | 6.5% |
Reaction Steps
A mixture of 4-(2,6-difluorobenzylamino)-1H-pyrazole-3-carboxylic acid (100 mg, 0.37 mmol) (Example 16D), 6-chloro-pyridine-3,4-diamine (54 mg, 0.37 mmol), EDC (72 mg, 0.40 mmol), HOBt (57.3 mg, 0.40 mmol) and Et3N (0.075 ml, 0.55 mmol) in DMF (20 ml) was stirred at ambient temperature for 48 h and then partitioned between EtOAc and saturated aqueous sodium bicarbonate and the organic portion dried (MgSO4), filtered and evaporated. The amide intermediate was dissolved in AcOH (3 ml), heated at reflux for 1 h, and then heated in the microwave (150 W) at 160° C. until the reaction was complete. The reaction mixture was allowed to cool, a solid crystallised out, which was filtered and then washed with petroleum ether and dried to give the required product (9 mg). (LC/MS: Rt 2.74, [M+H]+ 375)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977477B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-3cd9bfea20264e5cb6f277b84ad2b8a7 |
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| Source note | uspto-grants-2011_07 |
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