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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403093Generated: October 31, 2026

1-Hydroxybenzotriazole → 2-Amino-3-chlorobenzamide

https://huagongshe.com/reaction/1403093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Amino-3-chlorobenzoic acidHCID 80807—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantAzane;hydrateHCID 12896473—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Amino-3-chlorobenzamideHCID 1410042876.2%

Reaction Steps

EDCI hydrochloride (22.0 g) and 1-hydroxybenzotriazole (11.4 g) were added to a solution of 2-amino-3-chlorobenzoic acid (12.8 g) in DMF (100 mL), and subsequently ammonia water (22.0 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-chlorobenzamide (9.7 g). Iron(III) chloride hexahydrate (6.3 g) and cyclopropanecarbaldehyde (1.3 ml) were added to a suspension of the obtained 2-amino-3-chlorobenzamide (2.0 g) in water (30 ml), and the mixture was stirred overnight at 100° C. After cooling, water was added to the reaction solution, and the deposit was filtrated and dried under reduced pressure to obtain 8-chloro-2-cyclopropylquinazolin-4(1H)-one (2.0 g). Compound (115) was obtained as a yellow solid (yield based on 6 steps: 18%) according to Example 114(2) using the obtained 8-chloro-2-cyclopropylquinazolin-4(1H)-one instead of compound (114a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912181B2
Source datasetuspto-grants-2014_12
ORD IDord-3ab6aecc42324d8bb3aa832f8edf2b68
Source noteuspto-grants-2014_12