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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | (S)-tert-butyl((3-bromopyridin-2-yl)(4-(trifluoromethyl)phenyl)methyl)carbamate | HCID 71164782 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (S)-[2,3'-Bipyridin]-2'-yl(4-(trifluoromethyl)phenyl)-methanaminedihydrochloride | HCID 89621630 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778941B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-5905962cd45b4ceeb7c5955a5e3f1e4c |
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| Source note | uspto-grants-2014_07 |
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