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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068157Generated: October 25, 2026

1-(4-Piperidinyl)-1H-benzimidazole → HCID 86757025, compound

https://huagongshe.com/reaction/1068157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Piperidinyl)-1H-benzimidazoleHCID 3019262—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 54485407HCID 54485407—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86757025HCID 8675702572%

Reaction Steps

The title compound was prepared from 22 mg of α-(R)-(3-(R)-formyl-4-(S)-(3-fluorophenyl)pyrrolidin-1-yl)-3-cyclobutylpropionic acid, benzyl ester (prepared above as Aldehyde 2), 27 mg of 1-piperidin-4-yl-1-H-benzoimidazole (from Example 95, Step C) and 40 mg of sodium triacetoxyborohydride in 4 mL of THF and 1 mL of DMF, using a procedure analogous to that described in Example 95, Step D to provide 23 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248755B1
Source datasetuspto-grants-2001_06
ORD IDord-32f06224a7a649cb964effdd472865b7
Source noteuspto-grants-2001_06