Ethylenediamine → HCID 59548554, compound
Reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[C:4](F)[CH:3]=1.[CH2:12]([NH2:15])[CH2:13][NH2:14].F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.[OH-].[Na+]>C(Cl)Cl.CN(C=O)C>[Br:1][C:2]1[CH:10]=[CH:9][C:5]2[C:6](=[O:8])[NH:15][CH2:12][CH2:13][NH:14][C:4]=2[CH:3]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 4-Bromo-2-fluoro-benzoic acid (500 mg, 2.28 mmol) and 5 mL Ethane-1,2-diamine was reacted in a sealed tube under argon with microwave irradiation at 150 C for 30 min. The reaction was cooled, diluted with methylene chloride (200 mL), and DMF (10 mL) to give a homogeneous solution. 2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU), (1 g, 2.63 mmol, 1.1 eq.) was added, and the reaction stirred at room temperature for 2 hours. The reaction was then heated to 95 C for 15 hours, cooled, and 3 mL 5 N NaOH was added. The mixture was stirred at room temperature for 1 hour, the reaction was concentrated in vacuo, extracted with ethyl acetate 3×, the organic layers were dried and concentrated. The residue was purified by flash chromatography to give 150 mg of 8-Bromo-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one, 27%.
Workup
- customwas reacted in a sealed tube under argon with microwave irradiation at 150 C for 30 min
- temperatureThe reaction was cooled
- customto give a homogeneous solution
- temperatureThe reaction was then heated to 95 C for 15 hours
- temperaturecooled
- stirringThe mixture was stirred at room temperature for 1 hour
- concentrationthe reaction was concentrated in vacuo
- extractionextracted with ethyl acetate 3×
- customthe organic layers were dried
- concentrationconcentrated
- customThe residue was purified by flash chromatography
Sources & evidence
- ORD record
- ord-36cb8ebecd1e4602bed9b23e1eb49317
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318719B2
Reaction notes
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