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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374963Generated: October 30, 2026

Hydrochloric Acid → HCID 86592482, compound

https://huagongshe.com/reaction/1374963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 11765275HCID 11765275—
CatalystMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86592482HCID 8659248266.1%

Reaction Steps

To a solution of 336 mg (0.481 mmol) of 3-[({1-[5-(5-tert-Butyl-3-methanesulfonylamino-2-methoxy-phenylcarbamoyl)-2-methyl-phenyl]-1H-[1,2,3]triazole-4-carbonyl}-amino)-methyl]-piperidine-1-carboxylic acid tert-butyl ester (Example 72) in 5 mL CH2Cl2 was added dropwise 1.2 mL of 4N HCl in dioxane. As a gummy yellow precipitate began to form in the flask, 10 drops of MeOH were added and the solution was stirred overnight. The mixture was partitioned between CH2Cl2 (75 mL) and 50% saturated aqueous NaHCO3 (50 mL). The layers were separated and the aqueous portion was extracted with CH2Cl2 (2×30 mL). The combined extracts were washed with water (30 mL), brine (30 mL), dried (Na2SO4), filtered and concentrated to afford 190 mg of 1-[5-(5-tert-Butyl-3-methanesulfonylamino-2-methoxy-phenylcarbamoyl)-2-methyl-phenyl]-1H-[1,2,3]triazole-4-carboxylic acid (piperidin-3-ylmethyl)-amide as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166628B2
Source datasetuspto-grants-2007_01
ORD IDord-9b620197cdff4812ab4bb675a978c9bd
Source noteuspto-grants-2007_01