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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470319Generated: November 1, 2026

1-Hydroxybenzotriazole → HCID 178520339, compound

https://huagongshe.com/reaction/1470319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactantn-ChloroanilineHCID 258030—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178525222HCID 178525222—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178520339HCID 178520339—

Reaction Steps

To a solution of 2-(4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidin-5-yl)acetic acid, 12-d, (150 mg, 0.68 mmol) and HOBt (101.2 mg, 0.75 mmol) in DMF (5 ml) was added EDC.HCl (144 mg, 0.75 mmol) and DIEPA (264 mg, 2.05 mmol). The solution was stirred at room temperature for 5 mins before the addition of the chlorophenyl amine (0.75 mmol) (Sigma-Aldrich). The mixture was stirred at room temperature for 24 hours. The mixture was then diluted with water and extracted with ethyl acetate. The organic layer was concentrated under vacuum and the residue was purified by silica gel column or Prep-HPLC to give the final compound 12-1. 1H NMR (DMSO-d6, 300 MHz): δ 10.23 (s, 1H), 8.56 (d, 1H), 7.92 (s, 1H), 7.63 (d, 2H), 7.37 (d, 2H), 6.64 (s, 1H), 3.53 (s, 2H). (M+H)+=330.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006433B2
Source datasetuspto-grants-2015_04
ORD IDord-e19de86f8470455a86201044e41b580d
Source noteuspto-grants-2015_04