Hydrochloric Acid → 17-Allyl-3,14beta-dihydroxy-4,5beta-epoxy-6-methylamino-morphinan

HRID 651050Notes

Reaction equation

HRID 651050 reaction equation
[CH2:1]=[CH:2][CH2:3][N:4]1[C@@H:21]2[CH2:22][C:9]3[CH:10]=[CH:11][C:12]([OH:24])=[C:13]4[O:14][C@H:15]5[C:16]([CH2:18][CH2:19][C@:20]2([OH:23])[C@:7]5([C:8]=34)[CH2:6][CH2:5]1)=O.Cl.Cl.CN.[C:29]([BH3-])#[N:30].[Na+].Cl>CO>[CH2:3]([N:4]1[CH2:5][CH2:6][C@:7]23[C:8]4[C:13]5[O:14][C@H:15]2[C@@H:16]([NH:30][CH3:29])[CH2:18][CH2:19][C@@:20]3([OH:23])[C@H:21]1[CH2:22][C:9]=4[CH:10]=[CH:11][C:12]=5[OH:24])[CH:2]=[CH2:1].[CH2:3]([N:4]1[CH2:5][CH2:6][C@:7]23[C:8]4[C:13]5[O:14][C@@H:15]2[CH:16]([NH:30][CH3:29])[CH2:18][CH2:19][C@@:20]3([OH:23])[C@H:21]1[CH2:22][C:9]=4[CH:10]=[CH:11][C:12]=5[OH:24])[CH:2]=[CH2:1]

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 5003444Sodium cyanoborohydrideHCID 5464092Naloxone HydrochlorideHCID 6364545Methylamine hydrochloride

Product 2

HCID 5424824317-Allyl-3,14beta-dihydroxy-4,5alpha-epoxy-6alpha-methylaminomorphinanYield 12%HCID 7024349317-Allyl-3,14beta-dihydroxy-4,5beta-epoxy-6-methylamino-morphinanYield 24%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Naloxone hydrochloride (3.0 g), methylamine hydrochloride (5.57 g) and sodium cyanoborohydride (0.33 g) were suspended in anhydrous methanol (40 ml) and stirred for 17 hours at room temperature. After addition of concentrated hydrochloric acid (1.0 ml) and removal of solvent by distillation, distilled water (50 ml) was added followed by washing with chloroform (20 ml). Saturated aqueous sodium bicarbonate (10 ml) was added to make the solution basic followed by extraction with chloroform (30 ml×3). After drying with anhydrous magnesium sulfate, the solvent was distilled off. The resulting crude product was purified with silica gel column chromatography (Merk 7734 100 g; ethyl acetate/methanol/aqueous ammonia=90/10/1→80/20/2) to obtain the target compound in the form of a pure fraction (12 0.4 g, 12%; 13 0.8 g, 24%).

Workup

  1. distillationby distillation
  2. distillationdistilled water (50 ml)
  3. additionwas added
  4. washby washing with chloroform (20 ml)
  5. additionSaturated aqueous sodium bicarbonate (10 ml) was added
  6. extractionbasic followed by extraction with chloroform (30 ml×3)
  7. dry with materialAfter drying with anhydrous magnesium sulfate
  8. distillationthe solvent was distilled off
  9. customThe resulting crude product was purified with silica gel column chromatography (Merk 7734 100 g; ethyl acetate/methanol/aqueous ammonia=90/10/1→80/20/2)

Sources & evidence

ORD record
ord-5b5511ba64004eec886945ce61321a65
Source dataset
uspto-grants-2001_08
Patent number
US06277859B1

Reaction notes

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