Hydrogen Bromide → HCID 22475271, compound

HRID 1358102Notes

Reaction equation

HRID 1358102 reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([C:9]23[CH2:18][C:17]4[CH:19]=[CH:20][CH:21]=[CH:22][C:16]=4[CH2:15][C:14]2([CH3:23])[CH2:13][N:12]([CH3:24])[CH2:11][CH2:10]3)[CH:6]=[CH:7][CH:8]=1.Br.[OH-].[Na+].C([O-])(O)=O.[Na+]>C(O)(=O)C>[OH:2][C:3]1[CH:4]=[C:5]([C:9]23[CH2:18][C:17]4[CH:19]=[CH:20][CH:21]=[CH:22][C:16]=4[CH2:15][C:14]2([CH3:23])[CH2:13][N:12]([CH3:24])[CH2:11][CH2:10]3)[CH:6]=[CH:7][CH:8]=1

Participants

6

Reactant 4

HCID 260Hydrogen BromideHCID 14798Sodium HydroxideHCID 516892Sodium BicarbonateHCID 22475286HCID 22475286, compound

Product 1

HCID 22475271HCID 22475271, compoundYield 28.3%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

To a 10 mL single-necked flask was added 100 mg (0.31 mmol) of (±)-1,2,3,4,4a,5,10,10a-octahydro-4a-(3-methoxyphenyl)-2,10a-dimethylbenzo[g]isoquinoline (10) and 0.8 mL of glacial acetic acid and 0.8 mL of 48% HBr. This mixture was heated under reflux for 18 h and then cooled to room temperature. The pH was then adjusted to 10 with cooling starting with 50% NaOH and finishing with saturated NaHCO3. This was extracted 2 times with CHCl3 and 2 times with 3:1 n-butanol:toluene. Both extracts were dried over K2CO3, and then the solvent was removed. The material from both extracts was examined by 1H NMR and was shown to contain the desired product. The material from the CHCl3 layer was chromatographed on silica gel eluting with 25% CMA-80 in CHCl3. This gave 27 mg of the desired product (7) (28% yield). The residue was dissolved in MeOH, and to this was added 3 equivalents of 1N HCl in dry ethyl ether. The solvents were removed, and the residue crystallized from ether/MeOH. The butanol extracts contained 45 mg of the desired material giving an overall yield of 74.6%. MP ° C. 270-275 (dec). Anal. Calcd for C21H26NOCl.0.25H2O: C, 65.54; H, 7.20; N, 3.64. Found: C, 65.86; H, 7.15; N, 3.42. 1H NMR (DMSO) δ 1.014 (s, 3H); 1.587 (d, 1H, J=14.3 Hz); 2.072 (s, 3H); 2.358 (d, 1H, J=17.4 Hz); 2.498 (d, 1H, J=17.4 Hz); 2.734 (s, 3H); 2.924-2.792 (m, 3H); 3.113 (d, 1H, J=13.1 Hz); 3.602 (d, 1H, J=18.78 Hz); 6.562 (d, 1H, J=8.0 Hz); 6.611 (m, 2H); 6.993 (t, 1H, J=7.5 Hz); 7.081 (d, 1H, J=7.5 Hz); 7.148 (t, 1H, J=7.8 Hz); 7.269-7.193 (m, 2H); 9.30 (s, 1H); 9.898 (bs, 1H). 13C NMR (DMSO) δ 156.7, 146.4, 135.5, 133.3, 128.5, 128.4, 128.2, 126.2, 125.7, 117.6, 114.3, 113.5, 59.2, 49.4, 38.6, 35.4, 35.2, 31.0, 28.7, 22.8.

Workup

  1. temperatureThis mixture was heated
  2. temperatureunder reflux for 18 h
  3. temperaturewith cooling
  4. extractionThis was extracted 2 times with CHCl3 and 2 times with 3:1 n-butanol
  5. dry with materialBoth extracts were dried over K2CO3
  6. customthe solvent was removed
  7. customThe material from the CHCl3 layer was chromatographed on silica gel eluting with 25%

Sources & evidence

ORD record
ord-a10c9364444a4d7696c3918790b0a52d
Source dataset
uspto-grants-2003_07
Patent number
US06593348B2

Reaction notes

Loading…