HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiomorpholine → HCID 57839070, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | HCID 57839059 | HCID 57839059 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57839070 | HCID 57839070 | 101.8% |
Reaction Steps
To a stirred solution of methyl 2-(benzylsulfonyl)-4-(2,4-dichlorophenyl)-6-methylpyrimidine-5-carboxylate (17 mg, 0.037 mmol) in dioxane (2 mL) was added thiomorpholine (4.5 mL, 0.045 mmol). After at 40° C. for 1 hr, the reaction was concentrated under reduced pressure and diluted with EtOAc (10 mL). The organic layer was extracted with saturated NaHCO3 solution (2×6 mL), brine (5 mL), dried (MgSO4), filtered and concentrated under reduced pressure to give methyl 4-(2,4-dichlorophenyl)-6-methyl-2-thiomorpholinopyrimidine-5-carboxylate (15 mg, 100%). The crude reaction product (>98% purity) was moved onto next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589088B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-b71d6555c1474e0ab24c1a74475e59f9 |
| Source note | uspto-grants-2009_09 |