Cyanamide → HCID 25138704, compound
Reaction equation
[N+:1]([C:4]1[C:5]([NH2:13])=[CH:6][C:7]2[O:11][CH2:10][O:9][C:8]=2[CH:12]=1)([O-])=[O:2].[N:14]#[C:15][NH2:16].[CH]Cl.[OH-].[Na+]>O>[N+:1]1([O-:2])[C:4]2[CH:12]=[C:8]3[O:9][CH2:10][O:11][C:7]3=[CH:6][C:5]=2[N:13]=[C:15]([NH2:16])[N:14]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
A mixture of nitroaniline 220 (5.55 g, 30.5 mmol) and cyanamide (5.37 g, 122 mmol) were melted together at 100° C., cooled to 50° C., cHCl (15 mL) added dropwise and the mixture heated at 100° C. for 4 h. The mixture was cooled to 50° C., 7.5 M NaOH solution added until the mixture was strongly basic and the mixture stirred at 100° C. for 3 h. The mixture was cooled, diluted with water (200 mL), filtered, washed with water (3×30 mL), washed with ether (3×5 mL) and dried to give 1-oxide 221 (3.24 g, 51%) as a yellow powder: mp (MeOH/DCM) 290-295° C.; 1H NMR [(CD3)2SO] δ 7.45 (s, 1H, H-9), 7.00 (br s, 2H, NH2), 6.94 (s, 1H, H-5), 6.23 (s, 2H, H-7); 13C NMR [(CD3)2SO] δ 160.0, 155.1, 149.0, 147.0, 125.3, 103.1, 101.3, 95.8. Anal. calcd for CBH6N4O3: C, 46.6; H, 2.9; N, 27.2. Found: C, 46.7; H, 2.9; N, 27.3%.
Workup
- customwere melted together at 100° C.
- temperaturethe mixture heated at 100° C. for 4 h
- temperatureThe mixture was cooled to 50° C.
- temperatureThe mixture was cooled
- filtrationfiltered
- washwashed with water (3×30 mL)
- washwashed with ether (3×5 mL)
- customdried
Sources & evidence
- ORD record
- ord-66a9077a93c84d26abac1a88ac19f7e7
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989451B2
Reaction notes
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