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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212021Generated: October 30, 2026

1-Hydroxybenzotriazole → N-{[4-(3-fluorobenzyl)morpholin-2-yl]methyl}-2-{4-[(methylsulfonyl)amino]phenyl}acetamide

https://huagongshe.com/reaction/2212021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant{4-[(Methanesulfonyl)amino]phenyl}acetic acidHCID 2773887—
Reactant[4-(3-Fluorobenzyl)morpholin-2-yl]methylamineHCID 16244559—
SolventDimethylformamideHCID 6228—
ProductN-{[4-(3-fluorobenzyl)morpholin-2-yl]methyl}-2-{4-[(methylsulfonyl)amino]phenyl}acetamideHCID 21962840—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of Intermediate 29 (0.0134 g), {4-[(methylsulfonyl)amino]phenyl}acetic acid (0.0137 g, known compound WO 9929655 A1), 1-hydroxybenzotriazole (0.0097 g) and N,N-diisopropylethylamine (0.01 ml) in N,N-dimethylformamide (0.5 ml) was treated with a solution of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.00138 g) in N,N-dimethylformamide (0.5 ml). The mixture was stirred at 20° C. for 24 h. The mixture was partitioned between dichloromethane (4 ml) and saturated aqueous sodium hydrogen carbonate (4 ml). The phases were separated and the organic phase applied to an ion exchange cartridge (2 g Isolute SCX, prewashed with methanol). The SCX cartridge was eluted with methanol (10 ml) followed by 10% 0.880 ammonia in methanol (10 ml) and the appropriate fractions were concentrated in vacuo to give the title compoundas a colourless (0.0174 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101882B2
Source datasetuspto-grants-2006_09
ORD IDord-6c7f7aae084f4e3e8f0990dc74bd352f
Source noteuspto-grants-2006_09