Sodium Hydroxide → N-phenyl-1H-imidazol-2-amine
Reaction equation
C(O[CH:4](OCC)[CH2:5][NH:6][C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[NH:8])C.[OH-].[Na+]>Cl>[C:10]1([NH:9][C:7]2[NH:8][CH:4]=[CH:5][N:6]=2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The guanidine (b) was dissolved in HCl (5 mL, 6 M) at 0° C. and then stirred for 2 h. After the starting material was consumed, NaOH (25%) was added until a precipitate formed. This mixture was stirred for 30 min. The reaction was then poured into NaOH (0.5 M), extracted with CH2Cl2, dried and concentrated. Flash chromatography afforded (c) (0.95 g, 50%). 1H NMR (500 MHz, DMSO-d6) δ 8.58 (s, br, 1H), 7.34-6.74 (m, 5H), 6.68 (s, 2H), 6.62 (br, 2H), 3.82 (s, 6H), 3.73 (s, 3H). MS: 157.6 (M−H)−; 160.0 (M+H)+.
Workup
- customAfter the starting material was consumed
- additionNaOH (25%) was added until a precipitate
- customformed
- stirringThis mixture was stirred for 30 min
- extractionextracted with CH2Cl2
- customdried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-2cd5d24c2cfe43da8db53b5b7ce5c9c3
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09447049B2
Reaction notes
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