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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262042Generated: November 3, 2026

Hydrochloric Acid → 1-Methyl-4-[1-(4-nitro-phenyl)-piperidin-3-ylmethyl]-piperazine

https://huagongshe.com/reaction/1262042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoraneHCID 6331—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-3-yl]-methanoneHCID 66711465—
Product1-Methyl-4-[1-(4-nitro-phenyl)-piperidin-3-ylmethyl]-piperazineHCID 66711445—
Product1-Methyl-4-[1-(4-nitro-phenyl)-piperidin-4-ylmethyl]-piperazineHCID 66711733—

Reaction Steps

1-Methyl-4-[1-(4-nitro-phenyl)-piperidin-3-ylmethyl]-piperazine was prepared by warming (4-Methyl-piperazin-1-yl)-[1-(4-nitro-phenyl)-piperidin-3-yl]-methanone of Example 443a with borane.THF (10 equivalents) at 60° C. for 16 hours, followed by a standard aqueous HCl workup. The resulting aqueous phase was neutralized with NaHCO3 and extracted with EtOAc (2×). The organics were combined, dried over Na2SO4, filtered, and concentrated under reduced pressure to give 1-Methyl-4-[1-(4-nitro-phenyl)-piperidin-4-ylmethyl]-piperazine as an orange oil, which was used for subsequent step without further manipulation. LC/MS (E/I+) 319.18 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-ca31101ff3cf4f12b285fede964a4886
Source noteuspto-grants-2013_06