Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | HCID 86604161 | HCID 86604161 | — |
| Product | HCID 44430464 | HCID 44430464 | 30% |
Reaction Steps
A mixture of methanesulfonic acid 1-(6-azepan-1-yl-2-cyclopropyl-5-methyl-pyridin-4-yl)-azetidin-3-yl ester 190 (0.4 g, 1 mmol) and sodium bromide (0.103 g, 1 mmol) in N,N-dimethylformamide (10 ml) is heated at 100° C. for 6 days. The mixture is then cooled and concentrated in vacuo. The mixture is diluted with dichloromethane and washed two times with water. The combined organic layers are dried over magnesium sulfate and concentrated in vacuo to afford 0.4 g of a crude mixture, which is purified by column chromatography (dichloromethane/methanol 98/2). 1-[6-(3-bromo-azetidin-1-yl)-2-cyclopropyl-5-methyl-pyrimidin-4-yl]-azepane 182 (0.11 g, 30%) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07544675B2 |
|---|
| Source dataset | uspto-grants-2009_06 |
|---|
| ORD ID | ord-af097079104d45939befc49fca1deff9 |
|---|
| Source note | uspto-grants-2009_06 |
|---|