Ethylenediamine → HCID 59548554, compound

HRID 1879681Notes

Reaction equation

HRID 1879681 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]=1

Participants

7

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

  1. customwas reacted in a sealed tube under argon with microwave irradiation at 150 C for 30 min
  2. temperatureThe reaction was cooled
  3. customto give a homogeneous solution
  4. temperatureThe reaction was then heated to 95 C for 15 hours
  5. temperaturecooled
  6. stirringThe mixture was stirred at room temperature for 1 hour
  7. concentrationthe reaction was concentrated in vacuo
  8. extractionextracted with ethyl acetate 3×
  9. customthe organic layers were dried
  10. concentrationconcentrated
  11. customThe residue was purified by flash chromatography

Sources & evidence

ORD record
ord-36cb8ebecd1e4602bed9b23e1eb49317
Source dataset
uspto-grants-2012_11
Patent number
US08318719B2

Reaction notes

Loading…