Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen iodideHCID 24841—
Reactant2-(Tert-butoxy)ethanamineHCID 21914614—
Reactant(R)-(4-biphenylcarbonylamino)-2(R)-hydroxy-6-aminoindaneHCID 44185809—
Reactant(2-Tert-butoxyethyl)methyl-(1-methylsulfanylethyl)amineHCID 86607042—
SolventPyridineHCID 1049—
ProductBiphenyl-4-carboxylic acid (R)-(6-(1-((2-tert-butoxyethyl)methylamino)ethylideneamino)-2(R)-hydroxyindan-1-yl)amideHCID 5868945322%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378447B2
Source datasetuspto-grants-2008_05
ORD IDord-9e5c9b9d67914855a0914202de7e2192
Source noteuspto-grants-2008_05