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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184947Generated: November 1, 2026

Guanidine → tert-butyl (2S)-3-[4-(4-carbamimidamido-4-oxobutoxy)phenyl]-2-(phenylmethoxycarbonylamino)propanoate

https://huagongshe.com/reaction/2184947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidineHCID 3520—
Reactanttert-Butyl (2S)-2-benzyloxycarbonylamino-3-(4-(3-ethoxycarbonylpropyloxy)phenyl)propionateHCID 11038228—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (2S)-3-[4-(4-carbamimidamido-4-oxobutoxy)phenyl]-2-(phenylmethoxycarbonylamino)propanoateHCID 17845119042%

Reaction Steps

A solution of 3.64 g (61.69 mmol) of guanidine in 150 ml of tert-butanol was added to a solution of 20 g (41.23 mmol) of (1.1) in THF and the mixture was stirred at room temperature for 18 h. A further 4.5 g of guanidine in 150 ml of tert-butanol were then added, and the reaction solution was stirred at room temperature for 7 h, concentrated to about a half and stirred at room temperature for a further 18 h. The solvent was removed in vacuo and the residue was first filtered through basic Al2O3 using CH2Cl2/MeOH/H2O (95/5/0.5) and then chromatographed on silica gel by means of MPLC using CH2Cl2/MeOH/acetic acid (90/10/0.5). 8.6 g (42%) of (1.2) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399620B1
Source datasetuspto-grants-2002_06
ORD IDord-54ccd8a338674e0ebc135f78d36cad75
Source noteuspto-grants-2002_06