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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382423Generated: November 2, 2026

N-{(1S,2R,3S,4R)-4-[2-((R)-3-amino-pyrrolidin-1-yl)-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-propionamide → N-[(1S,2R,3S,4R)-4-[2-[(R)-3-(4,5-Dihydro-1H-imidazol-2-ylamino)-pyrrolidin-1-yl]-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl]-propionamide

https://huagongshe.com/reaction/2382423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-{(1S,2R,3S,4R)-4-[2-((R)-3-amino-pyrrolidin-1-yl)-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-propionamideHCID 59781437—
ReactantHCID 178506615HCID 178506615—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthanolHCID 702—
ProductN-[(1S,2R,3S,4R)-4-[2-[(R)-3-(4,5-Dihydro-1H-imidazol-2-ylamino)-pyrrolidin-1-yl]-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl]-propionamideHCID 24863901—

Reaction Steps

A mixture comprising N-{(1S,2R,3S,4R)-4-[2-((R)-3-amino-pyrrolidin-1-yl)-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-propionamide (Example 18 step 2) (30 mg, 0.053 mmol) and 4,5-dihydro-1H-imidazole-2-thiol hydroiodide (24 mg, 0.106 mmol) in absolute ethanol (2 ml) is treated with DMAP (catalytic amount) and TEA (29 μl, 0.212 mmol). The resulting mixture is heated using microwave radiation in a Personal Chemistry Emrys™ Optimizer microwave reactor at 150° C. for 4000 s. The solvent is removed in vacuo and purification of the crude product by preparative HPLC ((30-95% acetonitrile in water—0.1% TFA) affords the title compound. (MH+ 639.63)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258141B2
Source datasetuspto-grants-2012_09
ORD IDord-8b9c8c69520247149f8ac9e892e1d0d2
Source noteuspto-grants-2012_09