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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216011Generated: October 31, 2026

1,2-Dichloroethane → HCID 135749954, compound

https://huagongshe.com/reaction/216011

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantCyclopropylamineHCID 69828—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 1090984HCID 1090984—
SolventDichloromethaneHCID 6344—
ProductHCID 135749954HCID 13574995425%

Reaction Steps

To a 20 mL flask was added the crude acid from step 3 (20 mg, 0.1 mmol), HOBt (16 mg, 0.12 mmol), and EDC (23 mg, 0.12 mmol). To this was added dichloromethane (3 mL) and the resulting heterogeneous mixture was stirred for 30 minutes at room temperature. To the resulting solution was added cyclopropylamine (9.0 mg, 0.15 mmol) and the reaction was monitored by HPLC for product formation. After 2 hours, the reaction was complete and concentrated to a thick oil. This oil was partitioned between EtOAc (3 mL) and water (2 mL) with stirring for 10 minutes. The layers were then allowed to separate and the aqueous layer was discarded. The organic layer was then washed with water (2 mL), brine (2 ml) and dried over Na2SO4. Concentration gave an oil that was purified by column chromatography (30% EtOAc in hexanes) to give 6.1 mg (25% yield) of the desired isoxazole 6; 1H NMR (400 MHz, d6-DMSO)S 8.85 (d, 1H), 7.78 (d, 1H), 7.32 (t, 1H), 7.08 (s, 1H), 7.01 (d, 1H), 6.94 (t, 1H), 2.82 (m, 1H), 0.67 (m, 2H), 0.59 (m, 2H). LC/MS (electrospray ionization, positive mode) M+H=245.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193225B2
Source datasetuspto-grants-2012_06
ORD IDord-4aea3f249c8e4f6a8aee11d6075adb50
Source noteuspto-grants-2012_06