HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224744Generated: October 30, 2026
Hydrochloric Acid → Biphenyl-4-carboxylic acid (R)-(6-(1-((2-tert-butoxyethyl)methylamino)ethylideneamino)-2(R)-hydroxyindan-1-yl)amide
https://huagongshe.com/reaction/2224744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 2-(Tert-butoxy)ethanamine | HCID 21914614 | — |
| Reactant | (R)-(4-biphenylcarbonylamino)-2(R)-hydroxy-6-aminoindane | HCID 44185809 | — |
| Reactant | (2-Tert-butoxyethyl)methyl-(1-methylsulfanylethyl)amine | HCID 86607042 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Biphenyl-4-carboxylic acid (R)-(6-(1-((2-tert-butoxyethyl)methylamino)ethylideneamino)-2(R)-hydroxyindan-1-yl)amide | HCID 58689453 | 22% |
Reaction Steps
Dissolve the crude HI salt of (2-tert-butoxyethyl)methyl-(1-methylsulfanylethyl)amine (obtained using the crude HCl salt of 2-tert-butoxyethylamine, referenced in Example 9-1, using the methodology detailed in Example 6-1) (297.1 mg, 0.897 mmol) in 20 mL pyridine and add biphenyl-4-carboxylic acid (R)-(6-amino-2(R)-hydroxyindan-1-yl)amide (290.7 mg, 0.844 mmol). Allow the reaction to stir for 18 hours. Remove the solvent in vacuo and dissolve the residue in methylene chloride and wash with saturated aqueous sodium hydrogen carbonate. Dry the organic layer with magnesium sulfate. Filter and remove the solvent in vacuo to afford 248.7 mg of crude product. Purify the residue by Biotage chromatography (10% MeOH/EtOAc to 25% MeOH/EtOAc) to afford 91.7 mg of the titled product (22% yield). MS (ES): m/z 500.5 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07378447B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-9e5c9b9d67914855a0914202de7e2192 |
|---|
| Source note | uspto-grants-2008_05 |
|---|