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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042204Generated: November 3, 2026

1-Hydroxybenzotriazole → HCID 66726074, compound

https://huagongshe.com/reaction/1042204

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(2R)-1-aminopropan-2-olHCID 439938—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
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—
ProductHCID 66726074HCID 6672607478%

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 (R)-(−)-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 washed with ethyl acetate-hexane and recrystallized from tetrahydrofuran-ethyl acetate to give the title compound (264 mg, yield 78%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557805B2
Source datasetuspto-grants-2013_10
ORD IDord-dce4ee0cf3884e5194a98143cd7f2887
Source noteuspto-grants-2013_10