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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093308Generated: November 1, 2026

Trifluoroacetic acid → ((S)-5-amino-6-{(S)-2-[5-(4-fluoro-benzoyl)-pyridin-3-yl]pyrrolidin-1-yl}-6-oxo-hexyl)-carbamic acid 9H-fluoren-9-ylmethyl ester

https://huagongshe.com/reaction/2093308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant((S)-5-tert-butoxycarbonylamino-6-{(S)-2-[5-(4-fluoro-benzoyl)-pyridin-3-yl]-pyrrolidin-1-yl}-6-oxo-hexyl)-carbamic acid 9H-fluoren-9-ylmethyl esterHCID 58402903—
SolventDichloromethaneHCID 6344—
Product((S)-5-amino-6-{(S)-2-[5-(4-fluoro-benzoyl)-pyridin-3-yl]pyrrolidin-1-yl}-6-oxo-hexyl)-carbamic acid 9H-fluoren-9-ylmethyl esterHCID 67339553—

Reaction Steps

To a solution of ((S)-5-tert-butoxycarbonylamino-6-{(S)-2-[5-(4-fluoro-benzoyl)-pyridin-3-yl]-pyrrolidin-1-yl}-6-oxo-hexyl)-carbamic acid 9H-fluoren-9-ylmethyl ester (I-1a) in dichloromethane (15 mL) was added trifluoroacetic acid (5 mL). After stirring for 45 minutes, the reaction mixture was concentrated in vacuo to afford crude ((S)-5-amino-6-{(S)-2-[5-(4-fluoro-benzoyl)-pyridin-3-yl]pyrrolidin-1-yl}-6-oxo-hexyl)-carbamic acid 9H-fluoren-9-ylmethyl ester as a dark amber residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445440B2
Source datasetuspto-grants-2013_05
ORD IDord-b3e99406128a4b06ac3a342d789e1980
Source noteuspto-grants-2013_05