1,2-Dichloroethane → 6-[(4-Methylpiperazin-1-yl)methyl]pyridin-2-amine
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([CH:8]=O)[CH:5]=[CH:4][CH:3]=1.[CH3:10][N:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1.ClCCCl.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>>[CH3:10][N:11]1[CH2:16][CH2:15][N:14]([CH2:8][C:6]2[N:7]=[C:2]([NH2:1])[CH:3]=[CH:4][CH:5]=2)[CH2:13][CH2:12]1Participants
Procedure
Into a 1-neck round-bottom flask, 6-Amino-pyridine-2-carbaldehyde (2.85 g, 23.3 mmol), 1-Methylpiperazine (5.00 mL, 45.1 mmol), 1,2-Dichloroethane (100 mL, 1000 mmol) and Acetic acid (2.50 mL, 44.0 mmol) were added and stirred at room temperature for 2 hours. Sodium triacetoxyborohydride (14.8 g, 70.0 mmol) was added portion wise over 20 minutes. The reaction mixture was stirred at room temperature over night. The reaction was partitioned with Sat. NaHCO3. The organic was separated, washed with Brine and dried over Na2SO4. The solid was filtered and stripped to give a yellow solid. The reaction mixture was purified via ISCO column chromatography with DCM and methanol as eluant (0 to 20% methano). The collected fractions afforded 6-(4-Methyl-piperazin-1-ylmethyl)-pyridin-2-ylamine as a yellow solid (1.20, 25%)
Workup
- stirringThe reaction mixture was stirred at room temperature over night
- customThe reaction was partitioned with Sat. NaHCO3
- customThe organic was separated
- washwashed with Brine
- dry with materialdried over Na2SO4
- filtrationThe solid was filtered
- customto give a yellow solid
- customThe reaction mixture was purified via ISCO column chromatography with DCM and methanol as eluant (0 to 20% methano)
Sources & evidence
- ORD record
- ord-43a62c7dd93c47cd9a81dce7ce6578c8
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08471005B2
Reaction notes
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