Hydrochloric Acid → 6-(3-Chlorophenyl)-3-hexyl-6-methyl-3-azabicyclo[3.1.0]hexane

HRID 1826357Notes

Reaction equation

HRID 1826357 reaction equation
N([O-])=O.[Na+].[CH2:5]([N:11]1[CH2:16][CH:15]2[CH:13]([C:14]2([C:18]2[CH:19]=[C:20](N)[CH:21]=[CH:22][CH:23]=2)[CH3:17])[CH2:12]1)[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].C(=O)([O-])O.[Na+].[ClH:30]>O.[Cu]Cl>[Cl:30][C:20]1[CH:19]=[C:18]([C:14]2([CH3:17])[CH:15]3[CH:13]2[CH2:12][N:11]([CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH2:16]3)[CH:23]=[CH:22][CH:21]=1

Participants

7

Procedure

A solution of sodium nitrite (97 mg, 1.4 mmol) dissolved in water (2 ml) was added to 3-(3-hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamine (Preparation 12, 0.17 g, 0.61 mmol) dissolved in aqueous hydrochloric acid (2.0 M, 2 ml) over a few minutes at 0° C. After 30 min at 0° C., the reaction mixture was added to copper (I) chloride (1.57 g, 15.8 mmol) in concentrated hydrochloric acid (4.0 ml). After stirring the reaction mixture at room temperature for 45 min, the reaction mixture was heated to 90° C. for 5 min. The reaction mixture was poured cautiously on to solid, pre-wetted sodium hydrogen carbonate and the product was extracted firstly with diethyl ether and then ethyl acetate. The combined organic extracts were dried (MgSO4) and then concentrated in vacuo. The crude residue was purified by chromatography on silica gel eluting with hexane:ethyl acetate (8:1) to give the product (69 mg, 39%).

Workup

  1. temperaturethe reaction mixture was heated to 90° C. for 5 min
  2. extractionthe product was extracted firstly with diethyl ether
  3. dry with materialThe combined organic extracts were dried (MgSO4)
  4. concentrationconcentrated in vacuo
  5. customThe crude residue was purified by chromatography on silica gel eluting with hexane:ethyl acetate (8:1)

Sources & evidence

ORD record
ord-9e98f0cc32fb4b79af6643bf14ebb23a
Source dataset
uspto-grants-2006_05
Patent number
US07049444B2

Reaction notes

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