HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012168Generated: October 31, 2026
1,2-Dichloroethane → HCID 178486895, compound
https://huagongshe.com/reaction/1012168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 4-Methoxy-5-(4-methyl-piperidin-1-ylmethoxy)-benzene-1,2-diamine | HCID 67106286 | — |
| Reactant | HCID 178490649 | HCID 178490649 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178486895 | HCID 178486895 | 0.5% |
Reaction Steps
A mixture of 4-(5-Chloro-2-methoxy-benzoylamino)-1H-pyrazole-3-carboxylic acid (0.22 g, 0.745 mmol), 4-Methoxy-5-(4-methyl-piperidin-1-ylmethoxy)-benzene-1,2-diamine (0.2 g, 0.745 mmol), EDC (0.173 g, 0.89 mmol) and HOBt (0.122 g, 0.89 mmol) in DMF (20 ml) was stirred at 80° C. for 1 hour then at ambient temperature for 16 hours and then reduced in vacuo. The residue was partitioned between EtOAc and saturated bicarbonate, the organic portion was washed with brine and dried (MgSO4), filtered and evaporated. The amide intermediate (150 mg), (LC/MS (acidic method): Rt 2.13, [M+H]+ 543) was dissolved in AcOH (5 ml) then heated at reflux for 4 hours. The reaction mixture was allowed to cool, reduced in vacuo, residue purified by preparative TLC to yield 5-Chloro-2-methoxy-N-{3-[6-methoxy-5-(1-methyl-piperidin-4-ylmethoxy)-1H-benzimidazol-2-yl-]1H-pyrazol-4-yl}-benzamide (2 mg). (LC/MS (acidic method): Rt 2.25, [M+H]+ 525)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977477B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-9346cdf64545492589d5db45ab53d4f0 |
|---|
| Source note | uspto-grants-2011_07 |
|---|