Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloro-6-((methylsulfonyl)methyl)pyrimidine | HCID 57427625 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59379935 | HCID 59379935 | — |
Reaction Steps
A suspension of 2,4-dichloro-6-(methylsulfonylmethyl)pyrimidine (10.56 g) in DCM (230 mL) was stirred magnetically (under nitrogen) and cooled to −5° C. Triethylamine (6.78 mL) was added followed by the dropwise addition of a solution of morpholine (3.85 mL) in DCM (30 mL) maintaining the reaction temperature below −5° C. The reaction was stirred at room temperature for 1 hour and then the organic mixture washed with water (300 mL). The organic phase was dried (MgSO4), filtered and evaporated to a brown solid which was chromatographed on silica, eluting with 50% ethyl acetate in DCM, to give the desired material (6.81 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07750003B2 |
|---|
| Source dataset | uspto-grants-2010_07 |
|---|
| ORD ID | ord-7270175e13ef4bf69f933b203a3ffddc |
|---|
| Source note | uspto-grants-2010_07 |
|---|