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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502568Generated: November 4, 2026

Trifluoroacetic acid → HCID 58727170, compound

https://huagongshe.com/reaction/502568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68461104HCID 68461104—
SolventDichloromethaneHCID 6344—
ProductHCID 58727170HCID 58727170129.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl 2-(2-((3-(benzo[d]isothiazol-3-ylamino)propyl)((4′-methoxybiphenyl-4-yl)methyl)amino)-2-oxoethyl)pyrrolidine-1-carboxylate (20 mg, 0.033 mmol) was dissolved in methylene chloride (0.5 mL) and cooled in an ice-bath. A cooled solution of trifluoroacetic acid (1.0 mL) in methylene chloride (1.0 mL) was added to the mixture, dropwise. The reaction was allowed to stir for 3 h at 0° C. The solution was concentrated under reduced pressure to yield N-(3-(benzo[d]isothiazol-3-ylamino)propyl)-N-((4′-methoxybiphenyl-4-yl)methyl)-2-(pyrrolidin-2-yl) acetamide (22 mg) as a solid. 1H NMR (300 MHz, CDCl3): 8.15-8.20 (m, 1H), 7.45-7.70 (m, 6H), 7.15-7.20 (m, 2H), 6.90-6.95 (m, 2H), 4.60-4.75 (m, 1H), 4.45-4.55 (m, 1H), 3.95-4.10 (m, 2H), 3.85 (s, 3H), 3.60-3.75 (m, 2H), 3.35-3.45 (m,2H), 3.15-3.25 (m, 2H), 2.75-2.85 (m,1H), 1.90-2.00 ppm (m, 1H). MW=515 confirmed by LC-MS, tr=4.50 min (Method B) MH+=514-516.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776847B2
Source datasetuspto-grants-2010_08
ORD IDord-be36b18712b5492cacff996c92febe17
Source noteuspto-grants-2010_08