HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (s)-1-Chloro-3-(4-methylsulfonyl-1-piperazinyl)-2-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | 1-Piperazinesulfonamide | HCID 11252198 | — |
| Product | (s)-1-Chloro-3-(4-methylsulfonyl-1-piperazinyl)-2-propanol | HCID 44249051 | — |
Reaction Steps
(S)-Epichlorohydrin (48.0 mL, 0.612 mol) was added to a stirred solution of piperazine sulfonamide (87.3 g, 0.532 mol) in ethanol (1.33 L) at room temperature. The reaction mixture was stirred for 18 h and the white solid precipitate which formed was collected by filtration and washed with ethanol to afford the title intermediate (107.76 g) as a white solid which was used without further purification. (m/z): [M+H]+ calcd for C8H17ClN2O3S, 257.07; found 257.2. 1H NMR (DMSO-d6): δ (ppm) 2.37 (dd, 1H), 2.45 (dd, 1H), 2.50-2.58 (m, 4H), 2.86 (s, 3H), 3.09 (m, 4H), 3.55 (dd, 1H), 3.65 (dd, 1H), 3.84 (m, 1H), 5.09 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419989B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-9ec7ebc7c00949548bcf741cc7809e4a |
| Source note | uspto-grants-2008_09 |