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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502565Generated: November 3, 2026

4'-Methoxy-(1,1'-biphenyl)-4-carboxaldehyde → N1-(5-bromobenzo[d]isothiazol-3-yl)-N3-((4'-methoxybiphenyl-4-yl)methyl)propane-1,3-diamine

https://huagongshe.com/reaction/502565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-Methoxy-(1,1'-biphenyl)-4-carboxaldehydeHCID 1394487—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN1-(5-bromobenzo[d]isothiazol-3-yl)propane-1,3-diamineHCID 58726901—
CatalystAcetic AcidHCID 176—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
ProductN1-(5-bromobenzo[d]isothiazol-3-yl)-N3-((4'-methoxybiphenyl-4-yl)methyl)propane-1,3-diamineHCID 5872709240.8%

Reaction Steps

N1-(5-Bromobenzo[d]isothiazol-3-yl)propane-1,3-diamine (190 mg, 0.66 mmol) and 4′-methoxybiphenyl-4-carbaldehyde (140 mg, 0.66 mmol) were combined in 1,2-dichloroethane (30 mL) and treated with sodium triacetoxyborohydride (280 mg, 1.32 mmol) and acetic acid (one drop). The mixture was sonicated at room temperature for 18 h. The reaction was diluted with ethyl acetate and then washed with water, brine and saturated sodium bicarbonate solution. The organic solution was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography, on silica gel, eluting with 98:2 methylene chloride:methanol to yield N1-(5-bromobenzo[d]isothiazol-3-yl)-N3-((4′-methoxybiphenyl-4-yl)methyl)propane-1,3-diamine (130 mg) as a yellow solid. MW=482 confirmed by LC-MS, tr=3.24 min (Method B) MH+=481-483.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776847B2
Source datasetuspto-grants-2010_08
ORD IDord-2130aeb10882463fb20b6986130f3586
Source noteuspto-grants-2010_08