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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536689Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 58375169, compound

https://huagongshe.com/reaction/536689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58374955HCID 58374955—
SolventDichloromethaneHCID 6344—
ProductHCID 58375169HCID 58375169—

Reaction Steps

Trifluoroacetic anhydride (43 μL) is added to a solution of 3-(benzothiazole-6-carbonyl)-8-hydroxy-2,3,4,5-tetrahydro-1H-2,6-methano-benzo[d]azocine-6-carboxylic acid amide (40 mg) and ethyldiisopropylamine (50 μL) in dichloromethane (0.5 mL) chilled in an ice bath. The ice bath is removed and the solution is stirred at ambient temperature for 4 h. Then, another portion of trifluoroacetic anhydride (43 μL) and ethyldiisopropylamine (50 μL) are added and the solution is stirred overnight. Methanol (1 mL) is added and the solution is stirred for another 10 min. The solution is concentrated under reduced pressure and the residue is purified by HPLC on reversed phase (water/MeCN) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859580B2
Source datasetuspto-grants-2014_10
ORD IDord-aa87d82383b64fa0996550684c8f625b
Source noteuspto-grants-2014_10