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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4'-Methoxy-(1,1'-biphenyl)-4-carboxaldehyde | HCID 1394487 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N1-(5-bromobenzo[d]isothiazol-3-yl)propane-1,3-diamine | HCID 58726901 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N1-(5-bromobenzo[d]isothiazol-3-yl)-N3-((4'-methoxybiphenyl-4-yl)methyl)propane-1,3-diamine | HCID 58727092 | 40.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776847B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-2130aeb10882463fb20b6986130f3586 |
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| Source note | uspto-grants-2010_08 |
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