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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042203Generated: October 27, 2026

1-Hydroxybenzotriazole → N-[(2S)-2-Hydroxypropyl]-2-[2-(7-methyl-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indol-2-yl)-4,5-dihydro-1,3-thiazol-5-yl]acetamide

https://huagongshe.com/reaction/1042203

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(S)-(+)-1-Aminopropan-2-olHCID 7311736—
Reactant[2-(7-Methyl-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indol-2-yl)-4,5-dihydro-1,3-thiazol-5-yl]acetic acidHCID 58081062—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-[(2S)-2-Hydroxypropyl]-2-[2-(7-methyl-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indol-2-yl)-4,5-dihydro-1,3-thiazol-5-yl]acetamideHCID 6672608068%

Reaction Steps

To a solution of [2-(7-methyl-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indol-2-yl)-4,5-dihydro-1,3-thiazol-5-yl]acetic acid (300 mg) and (S)-(+)-1-amino-2-propanol (78 mg) in N,N-dimethylformamide (20 mL)were added 1-hydroxybenzotriazole (137 mg) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (194 mg) under ice-cooling, and the mixture was stirred under ice-cooling and then at room temperature for 15 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with aqueous sodium hydrogen carbonate solution and saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The obtained pale-yellow crystals were recrystallized from tetrahydrofuran-ethyl acetate to give the title compound (230 mg, yield 68%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557805B2
Source datasetuspto-grants-2013_10
ORD IDord-2700a00163144d48bd25919b19d21b9d
Source noteuspto-grants-2013_10