Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182176Generated: October 30, 2026

Trifluoroacetic acid → N-(3-Chloro-benzyl)-N-(3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-6'-yl)-acetamide

https://huagongshe.com/reaction/2182176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant6'-[Acetyl-(3-chloro-benzyl)-amino]-2,3,5,6-tetra-hydro-[1,2']bipyrazinyl-4-carboxylic acid tert-butyl esterHCID 69732327—
SolventDichloromethaneHCID 6344—
ProductN-(3-Chloro-benzyl)-N-(3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-6'-yl)-acetamideHCID 9924306126.3%

Reaction Steps

To a solution of 6′-[acetyl-(3-chloro-benzyl)-amino]-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid tert-butyl ester I-5c (27.1 mg, 0.06 mmol) in methylene chloride (1 mL) was added trifluoroacetic Acid (1 mL). The reaction mixture was stirred at room temperature until the reaction was completed. The reaction mixture was poured into saturated NaHCO3 (20 mL) and extracted with methylene chloride (2×15 mL). The organic layers were combined, dried (Na2SO4), filtered, and concentrated to dryness to yield the title compound 5-A (26.2 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894050B2
Source datasetuspto-grants-2005_05
ORD IDord-5ac56bed6b7b4a07b2e8365089018aea
Source noteuspto-grants-2005_05