HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → HCID 46865821, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 46865572 | HCID 46865572 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 46865821 | HCID 46865821 | — |
Reaction Steps
To a dimethylformamide solution of 450 mg of (S)-2-[1-(4-fluorophenyl)ethylamino]-6-(pyrazin-2-ylamino)isonicotinic acid (Example 141) and 2.2 ml of diisopropylamine was added, 1.32 g of 1H-benzotriazol-1-yloxy tripyrrolidinophosphonium hexafluorophosphate, and the mixture was stirred for 15 minutes. 520 mg of ethylamine hydrochloride was added thereto, and the mixture was stirred for 2 days. The reaction solution was diluted with ethyl acetate, and the organic layer was washed in turn with water and brine, and then dried over magnesium sulfate. The solvent was distilled off, and then the obtained residue was purified by silica gel column chromatography to obtain 390 mg of the objective compound as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586591B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-075fe7abfdff4c5ca251864e560013fa |
| Source note | uspto-grants-2013_11 |