Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 10550788 | HCID 10550788 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 10505924 | HCID 10505924 | 86.5% |
Reaction Steps
1-[[2-(Diethylamino)ethyl]amino]-4-(aminomethyl)-7-bromothioxanthen-9-one (1 g, 2.3 mmol) in 11.5 mL of dry pyridine under nitrogen was stirred in an ice bath for 15 min and 0.2 mL (2.6 mmol) of methanesulfonyl chloride in chilled pyridine was added dropwise and the mixture was stirred at room temperature. The reaction mixture was poured into 200 mL of water, added 0.19 g of sodium hydroxide in ice/water, and extracted into chloroform. The organic layer was washed with water (2x) and brine, and dried over anhydrous sodium sulfate. The mixture was filtered, concentrated in vacuo and the residue was stirred in ether, filtered, and dried to afford 1.02g of N-[[1-[[2-(diethylamino)ethyl]amino]-7-bromo -9-oxothioxanthen-4-yl]methyl]-methanesulfonamide, m.p. 134°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05665760 |
|---|
| Source dataset | uspto-grants-1997_09 |
|---|
| ORD ID | ord-21a33f0ddcdf432b852f8b741bb9e8d4 |
|---|
| Source note | uspto-grants-1997_09 |
|---|