HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 44219448, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 58277320 | HCID 58277320 | — |
| Reactant | HCID 58277360 | HCID 58277360 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 44219448 | HCID 44219448 | — |
Reaction Steps
The preparation of the title compound takes place starting from the compound of Example 110A using 3.2 equivalents of N,N-diisopropylethylamine and with the addition of 0.1% formic acid in the preparative HPLC in analogy to the synthesis of the compound of Example 23. In order to remove the 1,1′,1″-phosphoryltripyrrolidine the product is taken up in a little tetrahydrofuran, water is added to the mixture until a precipitate forms, the tetrahydrofuran is removed in vacuo, and the precipitate is collected by suction filtration and dried under high vacuum. 42 mg (65% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399682B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-d9a08a8d5d6b482d8b3899e483d058df |
| Source note | uspto-grants-2013_03 |