HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → (S)-1-isopropyl-4-[1-(tert-Butoxycarbonyl)-piperidine-4-carbonyl]-2-methyl piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid | HCID 392871 | — |
| Reactant | (S)-1-isopropyl-2-methyl piperazine hydrochloride | HCID 68816141 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-1-isopropyl-4-[1-(tert-Butoxycarbonyl)-piperidine-4-carbonyl]-2-methyl piperazine | HCID 68818623 | 96% |
Reaction Steps
1-(tert-Butoxycarbonyl)-piperidine4-carboxylic acid (3.2 g) in dry DMF (30 ml) was treated first with EDC (5.4 g) and catalytic HOAt followed by (S)-1-isopropyl-2-methyl piperazine hydrochloride (D27)(2 g) and N,N-diisopropylethylamine (5 ml). After the reaction mixture was stirred overnight, water (50 ml) was added and the cloudy precipitate was extracted into EtOAc (2×25 ml), dried (MgSO4) and filtered. The filtrate was absorbed on silica and purified by column chromatography [silica gel, step gradient 0-10% MeOH (containing 10% 0.88 ammonia solution) in DCM]. The fractions containing the required product were evaporated to give the title compound (D28) as an oil (3.8 g). LCMS electrospray (+ve) 354 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592347B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-16d4861e2e024ebea859845f34b0f8e8 |
| Source note | uspto-grants-2009_09 |