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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525036Generated: October 25, 2026

Disodium 2,3-dihydroxybutanedioate → (S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamate

https://huagongshe.com/reaction/525036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDisodium 2,3-dihydroxybutanedioateHCID 13355—
Reactant4-AminotetrahydropyranHCID 419223—
ReactantTrimethylaluminumHCID 16682925—
Reactant(S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylateHCID 86722033—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamateHCID 86722055—

Reaction Conditions

Temperature80 °C

Reaction Steps

Tetrahydro-2H-pyran-4-amine (900 microl, 8.69 mmols) was added to a solution of (S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylate (900 mg, 2.89 mmols, preparation 109) in toluene (36 ml). A 2M solution of Trimethyl aluminium in toluene (7 ml, 14.00 mmols) was added and it was stirred at 80° C. overnight. Water (50 ml) and a 0.5M solution of sodium tartrate (25 ml) were added. It was extracted with ethylacetate. The combined organic layers were washed with water and brine. It was dried, filtered and concentrated in vacuum. The title compound was obtained (617 mg, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340547B2
Source datasetuspto-grants-2016_05
ORD IDord-04de8d8e819c4455b3734c36e5918338
Source noteuspto-grants-2016_05