Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 3-(Methylsulfonyl)aniline hydrochloride | HCID 2735179 | — |
| Reactant | HCID 22022835 | HCID 22022835 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20356910 | HCID 20356910 | 55% |
Reaction Steps
To a solution of triphosgene (0.22 g, 0.33 eq.) in CH2Cl2 was added 3-methane-sulfonyl-phenylamine hydrochloride (0.5 g, 2.4 mmol), followed by the dropwise addition of TEA (0.37 ml, 1.1 eq.). The mixture was heated to 40° C. for 30 min. It was allowed to cool to rt and stirred for an additional 45 min. The isocyanate solution was then added to a solution of 2-[3-(4-chlorobenzyl)-8-aza-bicyclo[3.2.1]oct-8-yl]-1-methyl-ethylamine (0.18 g, 0.6 mmol) (prepared according to the procedure described in example 4, steps 1 to 4) in 6 ml of CH2Cl2. The mixture was stirred overnight at rt. It was diluted with CH2Cl2 and the organic layer was washed with Na2CO3 (sat.) twice, NaCl (sat.) and dried over Na2SO4. The crude mixture was purified on a silica-gel column with 1% iPrNH2, 9% MeOH in EtOAc to give 55% of Example 5 (M+: 490).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07081531B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-23f198ef4e9e47f1a2a8dd10acbcbbba |
|---|
| Source note | uspto-grants-2006_07 |
|---|