Aluminum(III) Chloride → 2-amino-9H-pyrido[2,3-b]indole-3-carboxamide

Temperature

95 °C

To a solution of 2-amino-9-benzyl-9H-pyrido[2,3-b]indole-3-carboxamide (vii-a, 1.01 g, 319 mmol) in benzene (30 mL) was added AlCl3 (1.10 g, 8.25 mmol), and the reaction was heated to 95° C. under atmosphere of Ar. After 6 h, the reaction was cooled to 0° C., quenched with water (75 mL) and poured into a separatory funnel containing EtOAc (200 mL). The mixture was washed with 1N NaOH (2×200 mL) and the organic layer was dried over sodium sulfate, filtered and concentrated to yield 2-amino-9H-pyrido[2,3-b]indole-3-carboxamide as a light brown solid (5, 319 mg, 44%). NH4OAc Standard conditions. DAD Retention Time=5.10 min. M+H=227. 1H NMR (300 MHz, DMSO-d6): δ 11.33 (br s, 1H), 8.68 (s, 1H), 7.85 (br s, 1H), 7.76 (d, J=7.9 Hz, 1H), 7.44 (br s, 1H), 7.32 (d, J=7.3 Hz, 1H), 7.24 (dd, J=7.3, 7.3 Hz, 1H), 7.12 (dd, J=7.9, 7.9 Hz, 1H).

1. temperaturethe reaction was cooled to 0° C.
2. customquenched with water (75 mL)
3. additionpoured into a separatory funnel
4. additioncontaining EtOAc (200 mL)
5. washThe mixture was washed with 1N NaOH (2×200 mL)
6. dry with materialthe organic layer was dried over sodium sulfate
7. filtrationfiltered
8. concentrationconcentrated

ORD record

ord-e30370e645a04a98ace9229a87690178

Source dataset

uspto-grants-2012_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08101604B2