Sodium hydride → 6-Bromo-1-(cyclohexylmethyl)-2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridine

Temperature

60 °C

NaHMDS (1 M solution in THF, 217 mL, 0.217 mmol) was added to a solution of 6-bromo-2-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[3,2-c]pyridine (Preparation 22, 50 mg, 0.180 mmol) in DMF (790 mL). The reaction mixture was then stirred for 10 minutes at room temperature before the addition of (bromomethyl)cyclohexane (38 mL, 0.271 mmol) and was stirred overnight at 60° C. NaH (60% in mineral oil) (14.4 mg, 0.361 mmol) and bromomethylcyclohexane (76 mL, 0.542 mmol) were then added. The reaction mixture was stirred for 1 hour at 60° C. before being diluted with water and EtOAc. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered and concentrated under reduced pressure. The crude was purified via Biotage silica gel column chromatography eluting with (DCM/EtOAc 99/1 to 80/20) to afford the title product as a colourless oil (40 mg, 59%). 1H NMR (500 MHz, CDCl3) d 0.84-0.94 (m, 2H), 1.06-1.17 (m, 3H), 1.43-1.50 (m, 2H), 1.61-1.69 (m, 3H), 1.70-1.78 (m, 1H), 3.95 (d, J=7.5 Hz, 2H), 4.02 (s, 3H), 6.52 (d, J=0.9 Hz, 1H), 7.41 (t, J=0.9 Hz, 1H), 7.57 (s, 1H), 7.66 (s, 1H), 8.58 (d, J=0.9 Hz, 1H). LC (Method B)-MS (ESI, m/z) tR 3.14 min, 373 [(M+H+), 100%].

1. stirringThe reaction mixture was stirred for 1 hour at 60° C.
2. customThe layers were separated
3. extractionthe aqueous layer was extracted with EtOAc
4. dry with materialThe combined organic layers were dried (Na2SO4)
5. filtrationfiltered
6. concentrationconcentrated under reduced pressure
7. customThe crude was purified via Biotage silica gel column chromatography
8. washeluting with (DCM/EtOAc 99/1 to 80/20)

ORD record

ord-715e4b0a7d7a409d8934d5dcde295c4b

Source dataset

uspto-grants-2016_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09371319B2