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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912720Generated: October 26, 2026

Trifluoroacetic acid → HCID 86631144, compound

https://huagongshe.com/reaction/912720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzoyl isothiocyanateHCID 68284—
Reactanttert-Butyl {2-[(5-carbamoyl-1H-imidazol-4-yl)amino]ethyl}carbamateHCID 86631143—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 86631144HCID 8663114467%

Reaction Conditions

Temperature80 °C

Reaction Steps

Benzoyl isothiocyanate (1.3 mL, 9.8 mmol) was added to tert-butyl {2-[(5-carbamoyl-1H-imidazol-4-yl)amino]ethyl}carbamate (2.5 g, 9.3 mmol, obtained from Example 26(a)) in dichloromethane (25 mL) and methanol (0.050 mL) at 0° C. The mixture was allowed to reach r.t. and stirred for 3 h. After removal of solvents, the residue was dissolved in ammonia (7 N in methanol, 30 mL) and subjected to microwave heating at 80° C. for 5 h. The solvent was then evaporated and the Boc-protected product was purified by silica gel column chromatography (dichloromethane/methanol 95:5) which gave 1.5 g (52% yield). This material (1.5 g, 4.9 mmol) was dissolved in dichloromethane (50 mL) and treated with trifluoroacetic acid (7 mL). After 2 h, the mixture was concentrated, diethyl ether was added and the solid was collected and dried in vacuo to afford 1.1 g (67% yield) of the title compound as its trifluoroacetic acid salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026244B2
Source datasetuspto-grants-2011_09
ORD IDord-6210b43854a04d468251d70fe31aa95f
Source noteuspto-grants-2011_09