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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487397Generated: October 30, 2026

Trifluoroacetic acid → HCID 68277224, compound

https://huagongshe.com/reaction/1487397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86680566HCID 86680566—
SolventDichloromethaneHCID 6344—
ProductHCID 68277224HCID 68277224137.6%

Reaction Steps

19.7 ml (25 eq) of trifluoroacetic acid is added to a solution of 4.72 g (10.23 mmol) of tert-butyl(S)-4-(3-(tert-butoxycarbonylamino)pyrrolidin-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)benzoate in 100 ml of dichloromethane. The reaction medium is stirred at room temperature for 30 hours. The solvents are evaporated and the residue is redissolved in diethyl ether and triturated until a solid is obtained. The solid formed is filtered and dried under vacuum to yield 4.3 g (100%) of a yellow powder of (S)-4-(3-aminopyrrolidin-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)benzoic acid in the form of a trifluoroacetic acid salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428510B2
Source datasetuspto-grants-2016_08
ORD IDord-493f5bcba0644689a53979b5d69af807
Source noteuspto-grants-2016_08