Structure of 932-57-0
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
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CAS No. : | 932-57-0 |
Formula : | C7H15NO |
M.W : | 129.20 |
SMILES Code : | O[C@H]1[C@@H](N)CCCCC1 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
77 mg | To a solution of 1-(4-fluorobenzyl)-1H-pyrrolo[3,2-b]pyridine-3-carboxylic acid (Intermediate 20), (110 mg) in DMF (2.1 mL) stirred at rt under nitrogen was added HATU (248 mg) and TEA (0.11 mL). This mixture was left to stir for 15 minutes and then <strong>[932-57-0]trans-2-aminocycloheptanol</strong> (52.6 mg) was introduced. The reaction was left to stir overnight at room temperature, at which point LC-MS indicated completion. The reaction mixture was transferred to a separating flask and EtOAc and water were added. The phases were separated and the aqueous phase was extracted twice more with EtOAc. The organic phases were combined and washed with brine. Solvent was removed in vacuo. The residue was purified by column chromatography (normal phase, 25 g, Biotage SNAP cartridge KP-Sil, 25 mL per min, gradient 0% to 100% EtOAc in hexane, followed by 0-15% MeOH/EtOAc) to give the desired product as a racemic mixture of trans isomers (77 mg). LCMS: m/z 382.60 [M+H]+. 1H NMR (400 MHz, CDCl3) ppm 1.41-2.02 (m, 10H) 3.77-3.92 (m, 1H) 4.07 (qd, J=7.4, 3.6 Hz, 1H) 5.22-5.36 (m, 2H) 6.94-7.21 (m, 5H) 7.60 (d, J=8.3 Hz, 1H) 8.06 (s, 1H) 8.50 (d, J=4.7 Hz, 1H) 9.18 (d, J=6.1 Hz, 1H). | |
77 mg | To a solution of 1-(4-fluorobenzyl)-1H-pyrrolo[3,2-b]pyridine-3-carboxylic acid (Intermediate 20), (110 mg) in DMF (2.1 mL) stirred at rt under nitrogen was added HATU (248 mg) and TEA (0.11 mL). This mixture was left to stir for 15 minutes and then <strong>[932-57-0]trans-2-aminocycloheptanol</strong> (52.6 mg) was introduced. The reaction was left to stir overnight at room temperature, at which point LC-MS indicated completion. The reaction mixture was transferred to a separating flask and EtOAc and water were added. The phases were separated and the aqueous phase was extracted twice more with EtOAc. The organic phases were combined and washed with brine. Solvent was removed in vacuo. The residue was purified by column chromatography (normal phase, 25 g, Biotage SNAP cartridge KP-Sil, 25 mL per min, gradient 0% to 100% EtOAc in hexane, followed by 0-15% MeOH/EtOAc) to give the desired product as a racemic mixture of trans isomers (77 mg). LCMS: m/z 382.60 [M+H]+. 1H NMR (400 MHz, CDCl3) ppm 1.41-2.02 (m, 10H) 3.77-3.92 (m, 1H) 4.07 (qd, J=7.4, 3.6 Hz, 1H) 5.22-5.36 (m, 2H) 6.94-7.21 (m, 5H) 7.60 (d, J=8.3 Hz, 1H) 8.06 (s, 1H) 8.50 (d, J=4.7 Hz, 1H) 9.18 (d, J=6.1 Hz, 1H). |