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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190345Generated: October 31, 2026

1,2-Dichloroethane → HCID 25175792, compound

https://huagongshe.com/reaction/2190345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMethylamineHCID 6329—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 25175638HCID 25175638—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 25175792HCID 25175792—

Reaction Steps

To a mixture of HOBt hydrate (0.042 g, 0.27 mmol), EDC (0.037 g, 0.19 mmol), and 3-(3-(5-chloro-4-(4-(methylsulfonamido)phenyl)thiazol-2-yl)-1-(3,3-diphenylpropyl)ureido)benzoic acid 78 (0.089 g, 0.13 mmol) was added DMF (1.5 mL). The reaction mixture was stirred at room temperature for 10 min and methylamine (2 mL, 2 M in MeOH, 4 mmol) was added. The reaction mixture was stirred at room temperature for 1 d and diluted with EtOAc. The organic phase was washed with water (1×), brine (1×), dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography on silica gel (eluted with 20% to 80% EtOAc in hexanes) gave 3-(((5-chloro-4-(4-((methylsulfonyl)amino)phenyl)-1,3-thiazol-2-yl)carbamoyl)(3,3-diphenylpropyl)amino)-N-methylbenzamide 79. Mass spectrum, calculated for C34H32ClN5O4S2 673.2; found 674.2 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324396B2
Source datasetuspto-grants-2012_12
ORD IDord-e9eb2a3272144ababe548cd15204e19a
Source noteuspto-grants-2012_12