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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983485Generated: October 30, 2026

Sodium triacetoxyborohydride → (7-Bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amine

https://huagongshe.com/reaction/983485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-(Methylsulfonyl)piperidine-4-carbaldehydeHCID 10954372—
Reactant(7-Bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amineHCID 17932068—
Solvent1,1-DichloroethaneHCID 6365—
Product(7-Bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amineHCID 1021686696.6%

Reaction Steps

To a solution of (7-bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine (536 mg, 2 mmol) and 1-methanesulfonyl-piperidine-4-carboxaldehyde (458 mg, 2.47mmol) in dichloroethane (10 mL) was added sodium triacetoxyborohydride (551 mg, 2.6 mmol) in a single portion. The reaction was stirred at room temperature for 24 h. The reaction was concentrated in vacuo and partitioned between EtOAc (75 mL) and 5% aq. KOH (75 mL). The organic layer was dried (MgSO4), filtered, and concentrated to afford (7-bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amine (857 mg) 111[M+H]+=444.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864266B2
Source datasetuspto-grants-2005_03
ORD IDord-ff7994eb085442788d5e0136aec2d8df
Source noteuspto-grants-2005_03