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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39834Generated: October 29, 2026

Dichloromethane → HCID 59398332, compound

https://huagongshe.com/reaction/39834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(piperidin-4-yl)carbamateHCID 57815320—
Reactant(7-Cyclohexyl-4-methyl-2-oxo-1,2-dihydroquinolin-1-yl)acetaldehydeHCID 59397891—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 59398332HCID 5939833260%

Reaction Steps

To 1.5 mL of dichloromethane solution containing 56 mg of (7-cyclohexyl-4-methyl-2-oxo-1,2-dihydroquinolin-1-yl)acetaldehyde, 69 mg of tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(piperidin-4-yl)carbamate and 15 μL of acetic acid were added, and stirred for 5 min. To the reaction mixture, 63 mg of sodium triacetoxyborohydride was added, and stirred for 45 min. Water and chloroform were added, the organic layer was separated, washed sequentially with water and aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=1:2], to give 73 mg of tert-butyl (1-(2-(7-cyclohexyl-4-methyl-2-oxo-1,2-dihydroquinolin-1-yl)ethyl)piperidin-4-yl)(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)carbamate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-2d1e9205980a4071b5dfdba4e5a98a8a
Source noteuspto-grants-2013_09