Chloroform → HCID 22791903, compound

HRID 2375510Notes

Reaction equation

HRID 2375510 reaction equation
C1(=O)[N:5]([CH2:6][CH2:7][CH2:8][O:9][C:10]2[CH:11]=[CH:12][C:13]3[CH2:14][C@H:15]4[N:27]([CH3:28])[CH2:26][CH2:25][C@:21]56[C:22]=3[C:23]=2[O:24][C@H:20]5[C@@H:19]([OH:29])[CH:18]=[CH:17][C@@H:16]46)C(=O)C2=CC=CC=C12.CN.C(Cl)(Cl)Cl>O>[NH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[CH2:14][C@H:15]3[N:27]([CH3:28])[CH2:26][CH2:25][C@:21]45[C:22]=2[C:23]=1[O:24][C@H:20]4[C@@H:19]([OH:29])[CH:18]=[CH:17][C@@H:16]35

Participants

5

Procedure

To 14 g (29.6 mmol) of 3O-phthalimidopropyl morphine (13) was added 188 mL of 2M ethanolic methylamine, and the reaction mixture was allowed to stir for 3.5 h at room temperature under nitrogen. The reaction mixture was poured into 650 mL of chloroform and 425 mL of cold water. The organic layer was separated, and the aqueous layer was extracted with 3×90 mL of chloroform. The chloroform layers were combined and extracted with 2×140 mL of 1N HCl. The aqueous extract was basified with 140 mL of 2.5 N NaOH and extracted with 3×300 mL of chloroform. The organic layer was dried (Na2SO4) and concentrated. The residue was crystallized from diethyl ether to give 8.9 g (26 mmol, 88%) of 14 as a white solid.

Workup

  1. customThe organic layer was separated
  2. extractionthe aqueous layer was extracted with 3×90 mL of chloroform
  3. extractionextracted with 2×140 mL of 1N HCl
  4. extractionThe aqueous extract
  5. extractionextracted with 3×300 mL of chloroform
  6. dry with materialThe organic layer was dried (Na2SO4)
  7. concentrationconcentrated
  8. customThe residue was crystallized from diethyl ether

Sources & evidence

ORD record
ord-4a68a56000fb40e180905554019bad43
Source dataset
uspto-grants-2008_12
Patent number
US07465797B2

Reaction notes

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