HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168892Generated: October 30, 2026
3-Aminophenylboronic acid → [7-(3-Amino-phenyl)-1,2,3,4-tetrahydro-naphthalen-2-yl]-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amine
https://huagongshe.com/reaction/1168892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Reactant | (7-Bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amine | HCID 10216866 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | [7-(3-Amino-phenyl)-1,2,3,4-tetrahydro-naphthalen-2-yl]-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amine | HCID 22989536 | — |
Reaction Steps
A 1 mL solution of (7-bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amine (25 mmole in DMA) was added to a tube containing 2-3 mg Pd(PPh3)4 catalyst followed by 120 μL of a solution of 3-amino phenyl boronic acid (30 mmole in DMA), and 200 μL 1N aq. NaOH. The solution was shaken at 80° C. for 4 h, concentrated, and purified by chromatography to yield [7-(3-amino-phenyl)-1,2,3,4-tetrahydro-naphthalen-2-yl]-(1-methanesulfonyl-piperidin-4-ylmethyl)-propyl-amine 112[M+H]+=456.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06627644B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-26954845ab494526b3f411e3dc0fb041 |
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| Source note | uspto-grants-2003_09 |
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