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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56762Generated: October 30, 2026

1H-Benzimidazole-2-carboxylic acid, 6-amino-, ethyl ester → Ethyl 6-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]butanoyl}amino)-1H-benzimidazole-2-carboxylate

https://huagongshe.com/reaction/56762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Benzimidazole-2-carboxylic acid, 6-amino-, ethyl esterHCID 45089720—
Reactant2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]butanoic acidHCID 117622569—
ProductEthyl 6-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]butanoyl}amino)-1H-benzimidazole-2-carboxylateHCID 117622570—

Reaction Steps

87 mg (0.25 mmol) of 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]butanoic acid (racemate) and 56 mg (0.28 mmol, 1.1 eq.) of ethyl 6-amino-1H-benzimidazole-2-carboxylate were reacted according to General Method 5A. The crude product was purified by preparative HPLC (Reprosil C18, acetonitrile/water+0.1% formic acid gradient). Yield: 86 mg (64% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434690B2
Source datasetuspto-grants-2016_09
ORD IDord-4bbf5adf92fb485584c7dd69008566a9
Source noteuspto-grants-2016_09