HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 22031350, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 22031009 | HCID 22031009 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22031350 | HCID 22031350 | 114.2% |
Reaction Steps
125 mg benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate, 1-hydroxy-1H-benzotriazole monohydrate, 83 mg diisopropylethylamine, and 18 mg ammonium chloride were added in this order to a mixture of 100 mg 4-{4-[3-(2-pyridyl)imidazo[1,2-a]pyridin-6-yl]-1-trityl-1H-3-pyrazolyl} benzoic acid obtained in Example 46 and 3 mL N,N-dimethylformamide, and the mixture was stirred at room temperature for 2 hour. Ethyl acetate and water were added to the reaction solution, the organic layer was separated, the solvent was evaporated, and the residue was purified by NH silica gel column chromatography (hexane/ethyl acetate) to give 114 mg of the title compound as a colorless amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074801B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-e731a84609504c2dbead9bf2573f28a6 |
| Source note | uspto-grants-2006_07 |