HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → H-Thz-NH-tBu
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 54130109 | HCID 54130109 | — |
| Solvent | Acetonitrile methylene chloride | HCID 21877088 | — |
| Product | H-Thz-NH-tBu | HCID 10535636 | 88% |
Reaction Steps
To a solution of 5.00 g (17.4 mmol) of Boc-Thz-NH-tBu in 23.7 ml of acetonitrile-dichloromethane (1:6), 3.39 ml (52.1 mmol) of methanesulfonic acid was added. After stirring at room temperature for 1.5 h, 30 ml of dichloromethane and 26 ml (52 mmol) of 2N NaOH aqueous solution were added under ice cooling to extract the product. The organic layer was washed with 5% NaHCO3 aqueous solution and saturated NaCl aqueous solution successively, dried over Na2SO4, and evaporated under reduced pressure. The residue was triturated in 50 ml of hexane to give 2.86 g (Y. 88%) of H-Thz-NH-tBu which was converted to Qoa-Mta-AHPBA-Thz-NH-tBu by a similar method with processes 3-5 of Example 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05644028 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-ca11e0de0ba743759c041a847e9bfb9c |
| Source note | uspto-grants-1997_07 |