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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403081Generated: October 27, 2026

1-Hydroxybenzotriazole → 2-Amino-3-iodobenzamide

https://huagongshe.com/reaction/1403081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Amino-3-iodobenzoic acidHCID 282070—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantAzane;hydrateHCID 12896473—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Amino-3-iodobenzamideHCID 6749745078.3%

Reaction Steps

EDCI hydrochloride (18.4 g) and 1-hydroxybenzotriazole (9.5 g) were added to a solution of 2-amino-3-iodobenzoic acid (16.4 g) synthesized using the method described in Journal of Medicinal Chemistry, 2004, 47 (6), 1448-1464 in DMF (120 mL), and subsequently ammonia water (21.2 ml) was added thereto. The reaction solution was stirred at room temperature for 3 hours. Water was added to the reaction solution, and the deposit was filtrated and dried under reduced pressure to obtain 2-amino-3-iodobenzamide (12.8 g). 60% sodium hydride (2.29 g) was added to a solution of the obtained 2-amino-3-iodobenzamide (5.0 g) in ethanol (95 ml), then ethyl trifluoroacetate (10.8 g) was added thereto, and the mixture was heated to reflux for 15 hours. After cooling, water was added thereto, and the reaction solution was rendered acidic by the addition of 6 N hydrochloric acid. Then, the deposit was filtrated and dried under reduced pressure to obtain compound (4a) (6.4 g, yield based on 2 steps: 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912181B2
Source datasetuspto-grants-2014_12
ORD IDord-d4a0ce7eb6a94a8684fdc9551a916d28
Source noteuspto-grants-2014_12