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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643696Generated: October 30, 2026

Pyridine → HCID 24750597, compound

https://huagongshe.com/reaction/643696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAmmonium BicarbonateHCID 14013—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantHCID 59253266HCID 59253266—
SolventAcetonitrileHCID 6342—
ProductHCID 24750597HCID 24750597100,160.703%

Reaction Steps

To a suspension of 2-{[1-(cyclopropylmethyl)-2-(2,2-dimethylpropyl)-1H-benzimidazol-5-yl]sulfonyl}-2-methylpropanoic acid (Step H, 200 mg, 0.51 mmol) and di-tert-butyl dicarbonate (145 mg, 0.66 mmol) in acetonitrile (3 mL) were added ammonium bicarbonate (48 mg, 0.61 mmol) and pyridine (48 mg, 0.61 mmol) at room temperature. The mixture was stirred at room temperature for 20 h and concentrated under reduced pressure. The residue was dissolved in water (30 mL) and dichloromethane (30 mL). The aqueous layer was separated and extracted with dichloromethane (30 mL). The combined organic layers were dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:3 as eluent) to afford the title compound (200 g, quant.) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700618B2
Source datasetuspto-grants-2010_04
ORD IDord-d0c0c58a94ec48a19b85caf4a639b68f
Source noteuspto-grants-2010_04