Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68027541 | HCID 68027541 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68029370 | HCID 68029370 | 30% |
Reaction Steps
To a solution of (R)—N2-methyl-N2-(1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-yl)pyridine-2,5-diamine (0.20 mmol) in DMF (5 mL) were added K2CO3 (0.24 mmol) and 1-Chloromethyl-4-fluoro-benzene (0.24 mmol) at room temperature. The mixture was stirred at 80° C. for 18 hours, poured into water and extracted with EtOAc. The organic layer was washed with water and brine sequentially, then concentrated. The residue was purified by preparative TLC to give the title compound in 30% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346810B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e65693a62c30443c9f9b663a0af2084c |
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| Source note | uspto-grants-2016_05 |
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