Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 68052115 | HCID 68052115 | — |
| Product | HCID 56967994 | HCID 56967994 | — |
Reaction Steps
To the product of Example 20 (40 mg, 0.102 mmol), was added HBr in acetic acid (1.5 mL, 0.102 mmol) and the reaction was stirred at room temperature for 2 hours before being concentrated in vacuo and azeotroped with heptanes (×2) and MeOH/heptanes (×1). The residue was taken up in methanol and passed through a Varian StratoSpheres™ SPE PL-HCO3 MP SPE resin. The solution was concentrated in vacuo and taken back up in MeOH (0.10 mL) and an additional amount of benzyl bromide (12.2 mg, 0.0714 mmol) was added and the reaction was stirred at 40° C. for 16 hours. The reaction was concentrated in vacuo and purified by mass triggered reverse phase HPLC. Lyophilization of the desired fractions gave the title product (TFA salt) as a white solid. LRMS calc'd for C21H26N5 [M+H]+, 348; found 348. Jak1 activity: ++.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937077B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-710729c60da64531bdd6ba63fb3cbfc6 |
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| Source note | uspto-grants-2015_01 |
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