Hydrochloric Acid → HCID 178422363, compound

HRID 726194Notes

Reaction equation

HRID 726194 reaction equation
C[O:2][C:3]1[C:4](=[O:17])[NH:5][C:6]2[CH:14]=[C:13]([CH3:15])[C:12]([CH3:16])=[CH:11][C:7]=2[C:8](=[O:10])[CH:9]=1.B(Br)(Br)Br.C([O-])(O)=O.[Na+].Cl>C(Cl)Cl.CCO>[OH:2][C:3]1[C:4](=[O:17])[NH:5][C:6]2[CH:14]=[C:13]([CH3:15])[C:12]([CH3:16])=[CH:11][C:7]=2[C:8](=[O:10])[CH:9]=1

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 10823398HCID 10823398, compound

Product 1

HCID 178422363HCID 178422363, compound

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 6344DichloromethaneSolvent

Procedure

To a stirred suspension of 3-methoxy-7,8-dimethyl-1H-1-benzazepine-2,5-dione (270 mg, 1.17 mmol) in dry CH2CH2 (2.7 mL, distilled from CaH2) under N2, there was added a solution of BBr3 in CH2Cl2 (2.7 mL, 1 M, Aldrich) in one portion over 20 seconds at rt. The reaction instantaneously became homogeneous and orange, then a brown precipitate formed after a few seconds. The reaction was allowed to stir under N2 at rt for 45 min. The reaction was added to saturated NaHCO3 (30 mL) and was allowed to stir for 15 min at rt to give a yellow suspension. The resulting suspension was acidified with concd HCl (pH 2), the acidic suspension stirred for 10 min at rt, the solid collected by filtration and washed to neutrality with water (6×4 mL). The damp filter cake was crystallized from 95% EtOH (dissolved in 550 mL, hot filtered, concd to 210 mL, allowed to cool to rt) to yield a fine yellow solid (195 mg, 77%, pure by TLC, 1H NMR and C,H,N analysis); mp 302°-304° C. (dec. EtOH) (lit 288° C. (dec) Birchall, G. R. et al. Can. J. Chem. 52:610-615 (1974)); 1H NMR (DMSO-d6) δ2.24 (d, 6H), 6.39 (s, 1H), 7.24 (s, 1H), 7.80 (s, 1H), 10.46 (s, 1H), 11.49 (s, 1H); Anal. Calcd for C12H11NO3 : C, 66.35; H, 5.10; N, 6.45. Found: C, 66.30; H, 4.88; N, 6.25.

Workup

  1. customThe reaction instantaneously became homogeneous
  2. customorange, then a brown precipitate formed after a few seconds
  3. stirringto stir for 15 min at rt
  4. customto give a yellow suspension
  5. stirringthe acidic suspension stirred for 10 min at rt
  6. filtrationthe solid collected by filtration
  7. washwashed
  8. customThe damp filter cake was crystallized from 95% EtOH (dissolved in 550 mL, hot filtered, concd to 210 mL, allowed to cool to rt)
  9. customto yield a fine yellow solid (195 mg, 77%, pure by TLC, 1H NMR and C,H,N analysis)

Sources & evidence

ORD record
ord-948911e98804465e932f18ced180e9e6
Source dataset
uspto-grants-1998_01
Patent number
US05708168

Reaction notes

Loading…