Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 68729453 | HCID 68729453 | — |
| Reactant | (S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine | HCID 68958720 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68725919 | HCID 68725919 | 11% |
Reaction Steps
Crude carbamimidate from step B (˜25 mg, 0.068 mmol), (S)-5-methyl-4-(3-methylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine, from Example 1, step B (16 mg, 0.68 mmol), and triethylamine (10 μl, 0.068 mmol) were combined in MeCN (0.5 ml) and heated to 70° C. for 2 hours. The mixture was concentrated and purified by preparative HPLC to afford (S)—N-(3-bromophenyl)-2-methyl-4-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N′-sulfamoylpiperazine-1-carboximidamide (4 mg, 0.0075 mmol, 11%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507672B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-bff76f12ba1b47fb8771f86fa96b557a |
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| Source note | uspto-grants-2013_08 |
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