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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064220Generated: November 1, 2026

Triethylamine → 5-Chloro-6-[(1-methylethyl)oxy]-1-[1-(tetrahydro-2H-pyran-4-yl)-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one hydrochloride

https://huagongshe.com/reaction/2064220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-Chloro-6-[(1-methylethyl)oxy]-1-(4-piperidinyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 59850186—
SolventDichloromethaneHCID 6344—
Product5-Chloro-6-[(1-methylethyl)oxy]-1-[1-(tetrahydro-2H-pyran-4-yl)-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one hydrochlorideHCID 6912857026,666.699%

Reaction Steps

A solution of 5-chloro-6-[(1-methylethyl)oxy]-1-(4-piperidinyl)-1,3-dihydro-2H-benzimidazol-2-one (D87, 94 mg, 0.30 mmol) in dichloromethane (3 ml) was treated with tetrahydro-4H-pyran-4-one (0.213 g, 0.21 mmol, 7 eq), sodium triacetoxyborohydride (0.445 g, 0.21 mmol, 7 eq) and triethylamine (0.101 g, 1 mmol, 3 eq) and stirred at room temperature under argon overnight. The mixture was diluted with dichloromethane and washed with aqueous NaOH solution (pH12). The NaOH wash was extracted with dichloromethane (×2) and the combined extracts was washed with aqu, NaOH solution, dried (MgSO4) and concentrated under vacuum. The residue was purified by MDAP to afford the title compound as a white solid (14 mg, 0.04 mol, 13%). M++H=394.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288412B2
Source datasetuspto-grants-2012_10
ORD IDord-74987ea991984770bbc8fb6155510f01
Source noteuspto-grants-2012_10