Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636814Generated: October 31, 2026

2-Amino-3-(1-trityl-1h-imidazol-4-yl)-2-(1-trityl-1h-imidazol-4-ylmethyl)-propionic acid methyl ester → 3-(3-Benzenesulfonyl-3-aza-bicyclo[3.1.0]hex-6-yl)-2-thioxo-5,5-bis-(1-trityl-1H-imidazol-4-ylmethyl)-imidazolidin 4one

https://huagongshe.com/reaction/636814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-(1-trityl-1h-imidazol-4-yl)-2-(1-trityl-1h-imidazol-4-ylmethyl)-propionic acid methyl esterHCID 15491433—
Reactant3-Benzenesulfonyl-6-isothiocyanato-3-aza-bicyclo[3.1.0]hexaneHCID 21255309—
Product3-(3-Benzenesulfonyl-3-aza-bicyclo[3.1.0]hex-6-yl)-2-thioxo-5,5-bis-(1-trityl-1H-imidazol-4-ylmethyl)-imidazolidin 4oneHCID 88218053—

Reaction Steps

Using the same procedure as described in Example 1B, the reaction mixture of the title compound of 53B (0.68 mmol) and 3-benzenesulfonyl-6-isothiocyanato-3-aza-bicyclo[3.1.0]hexane (6.71 mmol, prepared in 1A) was heated to reflux overnight under an atmosphere of dry N2. It was then poured into 10% K2CO3 aqueous solution and extracted with CH2Cl2. The organic layer was washed with brine, dried over MgSO4 and concentrated to afford the crude product. The crude product was chromatographed on silica gel with MeOH—CHCl3—NH4OH (1:99:0.1) as eluents to afford the title compound of 56B as a yellow solid, 0.548 g (0.558 mmol, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194438B1
Source datasetuspto-grants-2001_02
ORD IDord-d4b34b7d53c245d28ad728e7e0910486
Source noteuspto-grants-2001_02