Acetic Acid → HCID 178456794, compound

To a mixture of 1H-pyrazol-3-ylamine (8.3 g, 100 mmol), acetone (7.4 mL, 100 mmol) and acetic acid (12 mL, 200 mmol) in THF (280 mL) was added, in portions, sodium triacetoxyborohydride (27 g, 120 mmol) while cooling with an ice-water bath. The mixture was stirred at room temperature for 1 h and then at 50° C. for 3 h. After cooling to room temperature, 10 N NaOH (40 mL) was added dropwise, and stirred gently for 1 h. The clear solution was isolated with decantation. The gummy residue was washed with THF (2×50 mL). All the THF solutions were combined and concentrated. The residue was purified by silica gel column chromatography (EtOAc), affording isopropyl-(1H-pyrazol-3-yl)-amine (8.5 g, 68%) as a colorless oil. 1H NMR (300 MHz, CDCl3): δ 7.34 (d, 1H), 5.62 (d, 1H), 3.58 (m, 1H), 1.22 (d, 6H).

1. temperaturewhile cooling with an ice-water bath
2. waitat 50° C. for 3 h
3. temperatureAfter cooling to room temperature
4. stirringstirred gently for 1 h
5. customThe clear solution was isolated with decantation
6. washThe gummy residue was washed with THF (2×50 mL)
7. concentrationconcentrated
8. customThe residue was purified by silica gel column chromatography (EtOAc)

ORD record

ord-09b9c4392e6a4b419cc4ead3064393d7

Source dataset

uspto-grants-2014_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08809266B2