HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)benzyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (3-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenyl)methanol | HCID 68725684 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(5-(4-(Difluoromethoxy)phenyl)pyrimidin-2-ylamino)benzyl methanesulfonate | HCID 86660122 | — |
Reaction Steps
To a solution of (3-(5-(4-(difluoromethoxy)phenyl)pyrimidin-2-ylamino)phenyl)methanol 36 (6.22 mmol) in DCM (30 mL) is added triethylamine (9.33 mmol) and methanesulfonyl chloride (7.47 mmol). The reaction mixture is stirred at rt for 1.5 h. The reaction is diluted with H2O (10 mL) and washed with Na2CO3 solution (3×20 mL). The organic layer is washed with brine, dried over MgSO4 and concentrated to afford 3-(5-(4-(difluoromethoxy)phenyl)pyrimidin-2-ylamino)benzyl methanesulfonate 37. MS (m/z) (M+1)+422.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293757B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-cab46a8316724de298dbce131e4e10a4 |
| Source note | uspto-grants-2012_10 |