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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47589Generated: October 25, 2026

1,2-Dichloroethane → HCID 131724360, compound

https://huagongshe.com/reaction/47589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(R)-3-((tert-butoxycarbonyl)amino)-4-(3,4-difluorophenyl)butanoic acidHCID 7009791—
Reactant2-(trifluoromethyl)-5H,6H,7H,8H-imidazo[1,2-a]pyrazineHCID 14719928—
SolventDichloromethaneHCID 6344—
ProductHCID 131724360HCID 13172436099.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(trifluoromethyl)-5,6,7,8-tetrahydroimidazo[1,2-α]pyrazine (64.3 mg, 0.34 mmol, from Step B) and (3R)-3-[(1,1-dimethylethoxycarbonyl)amino]-4-(3,4-difluorophenyl)butanoic acid (105.9 mg, 0.34 mmol) in dichloromethane (5 mL) was added HOBT (54.5 mg, 0.42 mmol) at 0° C. The reaction was stirred at 0° C. for 10 min, then EDC (96.6 mg, 0.50 mmol) was added. After removal of the ice-bath, the reaction was allowed to stir at ambient temperature for 14 h. The mixture was concentrated and purified by HPLC (Gilson; YMC-Pack Pro C18 column, 100×20 mm I.D.; solvent gradient from 10% acetonitrile, 90% water, and 0.1% trifluoroacetic acid to 90% acetonitrile, 10% water, and 0.1% trifluoroacetic acid) to give 115 mg of the title compound as a foamy solid. 1H NMR (500 MHz, CDCl3) δ 1.36 (s, 9H), 2.62 (m, 2H), 2.86 (m, 2H) 3.34 (bs, 1H), 3.86 (m, 1H), 4.05 (m, 4H). 4.85 (m, 1H) 5.30-5.38 (m, 1H) 6.97 (m, 3H), 7.28 (m, 1H). LC/MS 489 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699871B2
Source datasetuspto-grants-2004_03
ORD IDord-6a8fcee6df9c48ffa1df32c6d014f5cd
Source noteuspto-grants-2004_03