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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382397Generated: October 25, 2026

3-Pyridineacetic acid, hydrochloride (1:1) → 1-benzyl-4-(3-(N-t-butyloxycarbonyl-N-methylamino)benzoylamino)-5-imidazole carboxamide

https://huagongshe.com/reaction/382397

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridineacetic acid, hydrochloride (1:1)HCID 2723724—
Reactant1-benzyl-4-amino-1H-imidazole-5-carboxamideHCID 14000620—
Reactant3-(N-Boc-N-methylamino)benzoic acidHCID 22349165—
Product1-benzyl-4-(3-(N-t-butyloxycarbonyl-N-methylamino)benzoylamino)-5-imidazole carboxamideHCID 1836049581%

Reaction Steps

An amidation reaction and post-treatment were carried out under the same conditions as in Example 17, using 0.65 g (3.0 mmol) of 4-amino-1-benzyl-5-imidazolecarboxamide which was prepared in the same manner as in Reference Example 2 and 3-(N-t-butyloxycarbonyl-N-methylamino)benzoic acid, instead of 3-pyridylacetic acid hydrochloride, to obtain 1.09 g of 1-benzyl-4-(3-(N-t-butyloxycarbonyl-N-methylamino)benzoylamino)-5-imidazole carboxamide (yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310070B1
Source datasetuspto-grants-2001_10
ORD IDord-e276764799474190a0415b2940ed430a
Source noteuspto-grants-2001_10