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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610811Generated: October 27, 2026

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

https://huagongshe.com/reaction/1610811

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 Conditions

Temperature65 °C

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. 0.3 M 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 CH2Cl2 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 numberUS06984627B1
Source datasetuspto-grants-2006_01
ORD IDord-b4d5ef07f20d45a792e35fa6284a44be
Source noteuspto-grants-2006_01