Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622562Generated: October 27, 2026

Hydrochloric Acid → (S)-[2,3'-Bipyridin]-2'-yl(4-(trifluoromethyl)phenyl)-methanaminedihydrochloride

https://huagongshe.com/reaction/1622562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(Tributylstannyl)pyridineHCID 607784—
Reactant(S)-tert-butyl((3-bromopyridin-2-yl)(4-(trifluoromethyl)phenyl)methyl)carbamateHCID 71164782—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product(S)-[2,3'-Bipyridin]-2'-yl(4-(trifluoromethyl)phenyl)-methanaminedihydrochlorideHCID 89621630—

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of (S)-tert-butyl(3-bromopyridin-2-yl)(4-(trifluoromethyl)-phenyl)methylcarbamate (Intermediate 40, Step 5) (0.711 g, 1.649 mmol), 2-(tributylstannyl)pyridine (0.910 g, 2.473 mmol), and (Ph3P)4Pd (0.381 g, 0.330 mmol) in 1,4-dioxane (10 mL) was heated by microwave at 125° C. for 30 min. The reaction mixture was then cooled, concentrated, and purified by ISCO (silica gel, 0-60% EtOAc/hexanes). The residue was dissolved in DCM (3 mL) and hydrogen chloride (3.30 mL, 13.19 mmol, 4.0 M in 1,4-dioxane) was added. After stirring for 2 h, the mixture was concentrated to dryness to give the title compound. MS (ESI pos. ion) m/z: 330.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778941B2
Source datasetuspto-grants-2014_07
ORD IDord-5905962cd45b4ceeb7c5955a5e3f1e4c
Source noteuspto-grants-2014_07