HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (RS)-S-[3-({5-bromo-4-[(R)-(2-hydroxy-1,2-dimethylpropyl)amino]pyrimidin-2-yl}amino)phenyl]-S-methyl sulfoximide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (R)-3-(5-bromo-2-chloropyrimidin-4-ylamino)-2-methylbutan-2-ol | HCID 59674068 | — |
| Reactant | 851008-24-7 | HCID 59674075 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (RS)-S-[3-({5-bromo-4-[(R)-(2-hydroxy-1,2-dimethylpropyl)amino]pyrimidin-2-yl}amino)phenyl]-S-methyl sulfoximide | HCID 59673989 | — |
Reaction Steps
127 mg (0.43 mmol) of (R)-3-[(5-bromo-2-chloropyrimidin-4-yl)amino]-2-methyl-butan-2-ol in 1 ml of acetonitrile is added to 74 mg (0.43 mmol) of (RS)—S-(3-aminophenyl)-S-methyl sulfoximide in 0.5 ml of acetonitrile. It is mixed with 0.1 ml of a 4N solution of HCl in dioxane, and the batch is refluxed overnight. The solvent is drawn off, and the remaining residue is purified by chromatography (DCM/EtOH 9:1). 37 mg (0.09 mmol, corresponding to 20% of theory) of the product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507510B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d90c49b4468b42cb8b9f7d05c1ec5df7 |
| Source note | uspto-grants-2013_08 |