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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727628Generated: October 30, 2026

Trifluoromethanesulfonate → (2S,4S)-4-Mercapto-2-[4-(N-4-nitrobenzyloxycarbonylformimidoyl)homopiperazin-1-ylcarbonyl]-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

https://huagongshe.com/reaction/727628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonateHCID 2758875—
Reactant(2S,4S)-4-(4-methoxybenzylthio)-2-(1-homopiperazinylcarbonyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine hydrochlorideHCID 22881639—
Reactant(4-nitrophenyl)methyl N-methanimidoylcarbamateHCID 140386401—
Product(2S,4S)-4-Mercapto-2-[4-(N-4-nitrobenzyloxycarbonylformimidoyl)homopiperazin-1-ylcarbonyl]-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 88300258—

Reaction Steps

Following a procedure similar to that described in Preparation 4, but using 2.10 g of (2S,4S)-4-(4-methoxybenzylthio)-2-(1-homopiperazinylcarbonyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine hydrochloride [prepared as described in Preparation 2(i)] and 0.93 g of N-(4-nitrobenzyloxycarbonyl)formamidine, 2.38 g of the trifluoromethanesulfonate of the title compound were obtained. The salt was treated by the same procedure as described in Preparation 4(ii), to give 1.90 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712267
Source datasetuspto-grants-1998_01
ORD IDord-d1dee884d94d4f0bbb2b175d2528009b
Source noteuspto-grants-1998_01