Hydrochloric Acid → HCID 86590685, compound

HRID 1823088Notes

Reaction equation

HRID 1823088 reaction equation
C(OC([N:8]([CH2:32][C@@H:33]([C:35]1[CH:40]=[CH:39][CH:38]=[C:37]([Cl:41])[CH:36]=1)[OH:34])[CH2:9][CH2:10][C:11]1[CH:31]=[CH:30][C:14]([O:15][CH2:16][C:17]2[CH:18]=[C:19]([CH:27]=[CH:28][CH:29]=2)[O:20][CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])=[CH:13][CH:12]=1)=O)(C)(C)C.Cl>O1CCCC1.O1CCOCC1>[Cl:41][C:37]1[CH:36]=[C:35]([C@@H:33]([OH:34])[CH2:32][NH:8][CH2:9][CH2:10][C:11]2[CH:12]=[CH:13][C:14]([O:15][CH2:16][C:17]3[CH:18]=[C:19]([CH:27]=[CH:28][CH:29]=3)[O:20][CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])=[CH:30][CH:31]=2)[CH:40]=[CH:39][CH:38]=1

Participants

5

Procedure

To a solution of ethyl [3-[[4-[2-[(tert-butoxycarbonyl)[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]-amino]ethyl]phenoxy]methyl]phenoxy]acetate (1.0 g) in tetrahydrofuran (5.0 ml) was added 4N hydrochloride in dioxane (4.3 ml). The mixture was stirred at room temperature for 8 hours and evaporated under reduced pressure. The residue was diluted with ethyl acetate and saturated sodium bicarbonate solution. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (methanol/chloroform=1/20) to give ethyl [3-[[4-[2-[[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]phenoxy]-methyl]phenoxy]acetate (632 mg).

Workup

  1. customevaporated under reduced pressure
  2. additionThe residue was diluted with ethyl acetate and saturated sodium bicarbonate solution
  3. customThe organic layer was separated
  4. washwashed with brine
  5. dry with materialdried over magnesium sulfate
  6. customevaporated under reduced pressure
  7. customThe residue was purified by column chromatography on silica gel (methanol/chloroform=1/20)

Sources & evidence

ORD record
ord-8620d975bdde48a8aee3fca4e2578256
Source dataset
uspto-grants-2006_05
Patent number
US07037938B2

Reaction notes

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