HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonyl-piperazin-1-yl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | n,n-Bis(2-chloroethyl)methanesulfonamide | HCID 245092 | — |
| Reactant | (R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)propanoate hydrochloride | HCID 51358429 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | methyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonyl-piperazin-1-yl)propanoate | HCID 67056910 | 44.1% |
Reaction Steps
A solution of 6 g (23.6 mmol) of methyl (R)-2-amino-3-tert-butoxycarbonylaminopropanoate hydrochloride and 5.2 g (23.6 mmol) of N,N-bis(2-chloroethyl)methanesulphonamide in 80 ml of N,N-diisopropylethylamine is heated at 125° C. with vigorous stirring for 18 h. After addition of water, the product is extracted with ethyl acetate. The organic phases are combined, washed with water, dried over magnesium sulphate, filtered and concentrated under vacuum. The crude product obtained is purified by chromatography over silica gel eluted with a 5/5 heptane/ethyl acetate mixture. 3.8 g (44%) of methyl (R)-3-tert-butoxycarbonylamino-2-(4-methanesulphonylpiperazin-1-yl)propanoate are obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115102B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9bb9523c700248b9a01547df2c48ab39 |
| Source note | uspto-grants-2015_08 |