HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → HCID 69138517, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride | HCID 3775717 | — |
| Reactant | HCID 18505313 | HCID 18505313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69138517 | HCID 69138517 | 95% |
Reaction Steps
Triethylamine (0.192 mL, 1.38 mmol) was added under nitrogen to a mixture of 5-bromo-6-methoxycarbonylmethoxy-naphthalen-2-ylmethyl-ammonium; chloride (0.25 g, 0.69 mmol), prepared in the previous step, and 1-phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride (0.17 g, 0.69 mmol) in 20 mL of methylene chloride at room temperature. The reaction stirred under nitrogen for 17 h. The reaction was diluted with methylene chloride, extracted two times with water, two times with 5% sodium bicarbonate, dried (MgSO4) and the solvent removed under reduced pressure to give (1-Bromo-6-{[(1-phenyl-5-propyl-1H-pyrazole-4-carbonyl)-amino]-methyl}-naphthalen-2-yloxy)-acetic acid methyl ester (0.347 g, 95%) as a white solid, mp 144-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06589970B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-b8dc005596b644aaa94d224b79ab2339 |
| Source note | uspto-grants-2003_07 |