Sodium hydride → HCID 15351906, compound

HRID 1858356Notes

Reaction equation

HRID 1858356 reaction equation
[H-].[Na+].[O:3]1[C@@H:15]2[C@@:16]34[CH2:18][CH2:19][N:20]([CH3:21])[C@@H:10]([C@@H:11]3[CH:12]=[CH:13][C@@H:14]2[OH:22])[CH2:9][C:8]2=[C:17]4[C:4]1=[C:5]([O:23][CH2:24][O:25][CH3:26])[CH:6]=[CH:7]2.Cl[C:28]1[N:38]=[CH:37][CH:36]=[CH:35][C:29]=1[C:30]([O:32][CH2:33][CH3:34])=[O:31]>CN(C=O)C>[O:3]1[C@@H:15]2[C@@:16]34[CH2:18][CH2:19][N:20]([CH3:21])[C@@H:10]([C@@H:11]3[CH:12]=[CH:13][C@@H:14]2[O:22][C:37]2[CH:36]=[CH:35][C:29]([C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:28][N:38]=2)[CH2:9][C:8]2=[C:17]4[C:4]1=[C:5]([O:23][CH2:24][O:25][CH3:26])[CH:6]=[CH:7]2

Participants

5

Procedure

NaH (0.72 g, 30 mmol) is stirred with absolute DMF (12 ml) at RT and then 4,5α-epoxy-3-methoxymethoxy-17-methyl-morphinan-7-en-6α-ol (1.9764 g, 6 mmol) in DMF (12 ml) is added. After the development of gas has ceased, a solution of ethyl 2-chloro-nicotinate (5.568 g, 30 mmol) in absolute DMF (8 ml) is added at RT. After 1 hour at RT this reaction mixture is poured onto H2O (100 ml) and extracted 3 times with CH2Cl2 (60 ml). The combined organic phases are dried with Na2SO4, concentrated by rotary evaporation and the residue is purified by flash chromatography (90 g silica gel, CH2Cl2MeOH=9/1). Yield: 2.53 g (5.29 mmol, 88%)

Workup

  1. additionAfter 1 hour at RT this reaction mixture is poured onto H2O (100 ml)
  2. extractionextracted 3 times with CH2Cl2 (60 ml)
  3. dry with materialThe combined organic phases are dried with Na2SO4
  4. concentrationconcentrated by rotary evaporation
  5. customthe residue is purified by flash chromatography (90 g silica gel, CH2Cl2MeOH=9/1)

Sources & evidence

ORD record
ord-d76bc52086264b008cb31afccdc2fe33
Source dataset
uspto-grants-2000_11
Patent number
US06150524

Reaction notes

Loading…