Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223921Generated: October 29, 2026

Sodium Bicarbonate → 1,3-Diacetoxymethyl-5-[2-[1-[2-[4-(5-methylpyridin-2-ylamino)piperidin-1-yl]ethyl]cyclohexyl]ethoxy]benzene

https://huagongshe.com/reaction/2223921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-Methyl-N-(piperidin-4-YL)pyridin-2-amineHCID 23021048—
Reactant1,3-Diacetoxymethyl-5-[2-[1-(formylmethyl)cyclohexyl]ethoxy]benzeneHCID 59714867—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
Product1,3-Diacetoxymethyl-5-[2-[1-[2-[4-(5-methylpyridin-2-ylamino)piperidin-1-yl]ethyl]cyclohexyl]ethoxy]benzeneHCID 5971497482.8%

Reaction Steps

1,3-Diacetoxymethyl-5-[2-[1-(formylmethyl)cyclohexyl]ethoxy]benzene (synthesized in Example 32) (215 mg) and 2-(piperidin-4-ylamino)-5-methylpyridine (synthesized in Preparation Example 4-3) (126 mg) were dissolved in 1,2-dichloroethane (5 mL). To this was added acetic acid (0.04 mL) at room temperature. The solution was stirred for 45 minutes. Sodium triacetoxyborohydride (295 mg) was added to the solution at room temperature and it was stirred for 3 hours. Saturated aqueous sodium bicarbonate solution was added to the solution and it was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and filtered. The filtrate was then concentrated under reduced pressure. The resulting residue was purified by chromatography [silica gel, chloroform-methanol (10:1)] to give the title compound (258 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375115B2
Source datasetuspto-grants-2008_05
ORD IDord-4f23d2b4373d4053a194413b57b9d4e1
Source noteuspto-grants-2008_05