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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324568Generated: October 30, 2026

Dichloromethane → HCID 178520177, compound

https://huagongshe.com/reaction/324568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBenzo-1,3-dioxole-5-acetic acidHCID 76115—
Reactanttert-butyl 3-amino-5-cyclopropyl-1H-pyrazole-1-carboxylateHCID 11218347—
SolventDiethyl EtherHCID 3283—
ProductHCID 178520177HCID 17852017763%

Reaction Steps

To a solution of 96.8 mg (0.537 mmol) of 2-(1,3-benzodioxol-5-yl)-acetic acid in 3 ml of dichloromethane 360 mg (0.720 mmol) of polystyrene supported dicyclohexylcarbodiimide (loading=2 mmol/g) and 40 mg (0.179 mmol) of tert-butyl-3-amino-5-cyclopropyl-1H-pyrazole-1-carboxylate were added. The mixture was maintained under stirring at room temperature for 96 hours and after that time filtered, washed several times with dichloromethane and evaporated to dryness. The residue was re-dissolved with 3 ml of trifluoroacetic acid 10% V/V in dichloromethane and maintained at room temperature for an hour. The solvent was then evaporated, the residue re-dissolved in dichloromethane and washed with a saturated solution of sodium hydrogenocarbonate. The organic layer was evaporated to dryness to give, after trituration with diethylether, 32 mg (63% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218418B1
Source datasetuspto-grants-2001_04
ORD IDord-66b315f6301c4a5fa704f65c43232bb6
Source noteuspto-grants-2001_04