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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957150Generated: October 27, 2026

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

https://huagongshe.com/reaction/1957150

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 14037908367,529.203%

Reaction Steps

2.18 g (0.0102 mmole) (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 numberUS05783563
Source datasetuspto-grants-1998_07
ORD IDord-c7a52d615e2c48989743433f4e761043
Source noteuspto-grants-1998_07