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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250391Generated: October 26, 2026

Diisopropylethylamine → N-(2-Amino-5-iodo-pyridin-3-yl)-3-[4-methyl-6-(trityl-amino)-pyridin-2-yl]-propionamide

https://huagongshe.com/reaction/2250391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Iodopyridine-2,3-diamineHCID 21882766—
Reactant3-[4-Methyl-6-(trityl-amino)-pyridin-2-yl]propionic acidHCID 68461590—
SolventPyridineHCID 1049—
ProductN-(2-Amino-5-iodo-pyridin-3-yl)-3-[4-methyl-6-(trityl-amino)-pyridin-2-yl]-propionamideHCID 6846109754.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

1.30 g of 3-[4-methyl-6-(trityl-amino)pyridin-2-yl]-propionic acid and 724 mg of 2,3-diamino-5-iodo-pyridine are dissolved in 37 ml of pyridine and sequentially treated with 1.06 g of O-[(ethoxycarbonyl)canomethylene-amino]-N,N,N′,N′-tetramethyl-uronium tetrafluoroborate and 579 μl of diisopropylethyl amine. The reaction mixture is warmed to 50° C. for 24 h. Thereafter the solvents are evaporated in vacuo. The remaining residue is coevaporated twice with toluene yielding 3.55 g of crude product. Purification by chromatography on LiChroprep® NH2 (25-40 μm, Merck, Darmstadt) (75 g, eluent: toluene/ethyl acetate 1:1) affords 1.08 g of the title compound as an amorphous solid. ESI-MS: 640.0 (MH+). TLC: Rf=0.16 (toluene/ethyl acetate 1:1, LiChroprep® NH2 HPTLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317021B2
Source datasetuspto-grants-2008_01
ORD IDord-263ea1d8e1cc466681738b6da5ab972b
Source noteuspto-grants-2008_01