Methylhydrazine → 2-Bromo-6-(1-methylhydrazinyl)pyridine
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4](Br)[N:3]=1.[CH3:9][NH:10][NH2:11]>>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N:10]([CH3:9])[NH2:11])[N:3]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
A suspension of 2,6-dibromopyridine (10.0 g, 42.0 mmol) in anhydrous methylhydrazine (10 mL) was heated at 100° C. for 2 h. The mixture was cooled to room temperature and washed with water (3×20 mL). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, hexanes/EtOAc, 80:20) gave the title compound (5.70 g, 66%) as white solid: 1H NMR (500 MHz, CDCl3) δ 7.30-7.26 (dd, J=8.5, 7.8 Hz, 1H), 6.83 (d, J=8.0 Hz, 1H), 6.73 (d, J=7.0 Hz, 1H), 4.03 (br s, 2H), 3.36 (s, 3H).
Workup
- temperatureThe mixture was cooled to room temperature
- washwashed with water (3×20 mL)
- dry with materialThe combined organic extracts were dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customPurification by flash column chromatography (silica gel, hexanes/EtOAc, 80:20)
Sources & evidence
- ORD record
- ord-c688e6500bc0419abc42bef1a53db9b1
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08629158B2
Reaction notes
Loading…