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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385891Generated: October 30, 2026

Carbodiimide → 6-({3-(Aminocarbonyl)-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-thienyl}amino)-N-(oxetan-2-ylmethyl)pyridine-2-carboxamide

https://huagongshe.com/reaction/385891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbodiimideHCID 160435—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant1-(Oxetan-2-yl)methanamineHCID 20293931—
Reactant6-({3-(Aminocarbonyl)-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-thienyl}amino)pyridine-2-carboxylic acidHCID 25123167—
SolventDimethylformamideHCID 6228—
Product6-({3-(Aminocarbonyl)-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-thienyl}amino)-N-(oxetan-2-ylmethyl)pyridine-2-carboxamideHCID 59525937—

Reaction Steps

A mixture of 6-({3-(aminocarbonyl)-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-thienyl}amino)pyridine-2-carboxylic acid (Table 3, Example 40) (50 mg, 0.12 mmol), 1-oxetan-2-ylmethanamine (11 mg, 0.12 mmol), 1-hydroxybenzotriazole hydrate (22 mg, 0.14 mmol), and PS-Carbodiimide (240 mg, 0.30 mmol, 1.25 mmol/g) in DMF (4 mL) was irradiated in a microwave at 100° C. for 10 minutes. Upon completion, the crude reaction was filtered, concentrated, and purified by silica gel chromatography (0-7% methanol/ethyl acetate) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-928add3b9c154b4d95953e006a094402
Source noteuspto-grants-2013_02