Hydrochloric Acid → HCID 57803347, compound

HRID 2103358Notes

Reaction equation

HRID 2103358 reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]2([OH:21])[CH2:20][CH2:19][C:14]3(OCC[O:15]3)[CH2:13][CH2:12]2)=[N:9][CH:10]=1)[CH3:3].Cl.C([O-])(O)=O.[Na+]>C1COCC1>[CH3:3][N:2]([CH2:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]2([OH:21])[CH2:20][CH2:19][C:14](=[O:15])[CH2:13][CH2:12]2)=[N:9][CH:10]=1)[CH3:1]

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 578034018-[5-[(Dimethylamino)methyl]-2-pyridinyl]-1,4-dioxaspiro[4.5]decan-8-ol

Product 1

HCID 57803347HCID 57803347, compoundYield 51.4%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

8-{5-[(Dimethylamino)methyl]pyridin-2-yl}-1,4-dioxaspiro[4,5]decan-8-ol (0.85 g, 2.9 mmol) was dissolved in 10 mL of THF and 10 mL of 2 N HCl solution was added. After being stirred for two hours, the reaction mixture was neutralized to pH˜8-9 by addition of a saturated NaHCO3 aqueous solution and extracted twice using EtOAc. The combined extracts were dried and concentrated to obtain 0.37 g white solid (51% yield), MS: (M+H)+ 249.2.

Workup

  1. extractionextracted twice using EtOAc
  2. customThe combined extracts were dried
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-039d43f2310a4dd7811ca70b92badd96
Source dataset
uspto-grants-2009_08
Patent number
US07576089B2

Reaction notes

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