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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522349Generated: October 29, 2026

Trifluoroacetic acid → (1R,2S)-1-amino-2-ethenyl-N-{[-(methoxymethyl)cyclopropyl]sulfonyl}cyclopropanecarboxamide trifluoroacetate

https://huagongshe.com/reaction/522349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl [(1R,2S)-2-ethenyl-1-({[1-(methoxymethyl)cyclopropyl]sulfonyl}carbamoyl)cyclopropyl]carbamateHCID 131735528—
SolventDichloromethaneHCID 6344—
Product(1R,2S)-1-amino-2-ethenyl-N-{[-(methoxymethyl)cyclopropyl]sulfonyl}cyclopropanecarboxamide trifluoroacetateHCID 117598869—

Reaction Steps

To a 0° C. solution of the product of Step 1 (120 mg) in DCM (1 mL) at 0° C. was added TFA (1 mL). The mixture was slowly warmed to room temperature and stirred for 3 hours. The solvent was removed in vacuo and the crude product was used in the next step. 1H NMR (400 MHz, CDCl3): δ (ppm) 5.82 (ddd, 1H), 5.44 (d, 1H), 5.43 (d, 1H), 3.67 (d, 1H), 3.63 (d, 1H), 3.35 (s, 3H), 2.64 (dt, 1H), 1.92 (dd, 1H), 1.83 (dd, 1H), 1.76-1.70 (m, 1H), 1.67-1.60 (m, 1H), 1.14-1.02 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328138B2
Source datasetuspto-grants-2016_05
ORD IDord-3ec1e32d4546440891442a217a74ede0
Source noteuspto-grants-2016_05