Formaldehyde → 1-[(4-Aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)methyl]piperidin-4-ol

4-Hydroxypiperidine (3.62 g, 35.8 mmol) and 37% formalin solution (2.9 g, 35.8 mmol) were dissolved in acetic acid (150 mL) and stirred at room temperature for 1 h. To this solution was added a solution of pyrrolo[2,1-f][1,2,4]triazin-4-amine (2.0 g, 14.9 mmol; prepared according to the procedure described in WO 2007/056170-A2, Intermediate A) in acetic acid (150 mL), and the mixture was stirred at 60° C. for 2 h. The solvent was then evaporated, and the residue was taken up in 200 mL of half-concentrated aqueous potassium bicarbonate solution and extracted with 200 mL dichloromethane. The organic layer was washed with water (2×50 mL) and discarded. The combined aqueous layers were evaporated to dryness, and the residue was treated with a 10:1 mixture of dichloromethane and methanol (2×100 mL). The organic extracts were evaporated, and the residue was purified by preparative HPLC (method 4) to give 1.16 g (15% of th.) of the title compound.

1. customprepared
2. stirringthe mixture was stirred at 60° C. for 2 h
3. customThe solvent was then evaporated
4. extractionextracted with 200 mL dichloromethane
5. washThe organic layer was washed with water (2×50 mL)
6. customThe combined aqueous layers were evaporated to dryness
7. additionthe residue was treated with a 10:1 mixture of dichloromethane and methanol (2×100 mL)
8. customThe organic extracts were evaporated
9. customthe residue was purified by preparative HPLC (method 4)

ORD record

ord-7e7482553e8e4edd8db40ac69c3e3fe9

Source dataset

uspto-grants-2015_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09040691B2