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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869Generated: October 25, 2026

Potassium bisulfate → benzyl N-[3-(2-aminoethyl)pyrrolidine-1-carboximidoyl]carbamate

https://huagongshe.com/reaction/869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
Reactanttert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamateHCID 21955469—
ReactantBenzyl [amino(methylsulfanyl)methylene]carbamateHCID 140362141—
SolventTolueneHCID 1140—
Productbenzyl N-[3-(2-aminoethyl)pyrrolidine-1-carboximidoyl]carbamateHCID 14037908367.5%

Reaction Steps

2.18 g (0.0102 mole) (3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine and 2.81 g (0.0125 mole) N-benzyloxycarbonyl-S-methylisothiourea was dissolved in 30 ml toluene and heated to 60°-70° C. for eight hours followed by stirring at room temperature for one day. 0.3M KHSO4 -solution was added and the water layer was washed with a mixture of the toluene and ethyl acetate and left for 2 days under which time the Boc group was removed. The acidic water phase was made alkaline and extracted four times with CH2 Cl2. The combined organic layer was dried (Na2SO4), filtered and evaporated to yield 2.0 g (51%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723444
Source datasetuspto-grants-1998_03
ORD IDord-d42f48a7d3fc473aba6c5139093935b5
Source noteuspto-grants-1998_03