Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(3-Amino-4-methylphenyl)-N~2~,N~2~-dimethylglycinamide | HCID 17607975 | — |
| Reactant | HCID 25150094 | HCID 25150094 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67316367 | HCID 67316367 | 823.8% |
Reaction Steps
To a pressurized vessel was added 2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)benzamide (1.0 g, 2.27 mmol), N1-(3-amino-4-methylphenyl)-N2,N2-dimethylglycinamide (0.590 g, 2.83 mmol), potassium iodide (<10 mg) and hydrochloric acid as a 4.0M solution in dioxanes (ca 4 mL). The resulting suspension was stirred until all solids had completely dissolved (24 hr.) The reaction was poured into into saturated sodium bicarbonate and diluted with dichloromethane. The organic layer was dried over sodium sulfate, volatiles removed under reduced pressure, and the solids triturated with diethyl ether to afford N2,N2-dimethyl-N1-[4-methyl-3-({3-[(4-methylphenyl)sulfonyl]-7-oxo-3,7-dihydropyrrolo[2′,3′:4,5]pyrimido[6,1-b]quinazolin-5-yl}amino)phenyl]glycinamide (1.11 g, 18.7 mmol, 82% yield) of sufficient purity for use in subsequent transformations. ESIMS (M+H)=596.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07981903B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-d54ebd19625045e58ed574fbbbb7f8e3 |
|---|
| Source note | uspto-grants-2011_07 |
|---|