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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051885Generated: November 1, 2026

1,2-Dichloroethane → HCID 89813286, compound

https://huagongshe.com/reaction/1051885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
Reactant4-(4-Chlorophenyl)-1,3-thiazole-2-carboxylic acidHCID 16064919—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 89813286HCID 8981328632.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(4-chlorophenyl)thiazole-2-carboxylic acid (prepared according to the procedure given in US 2007/32531, 1.00 g, 4.17 mmol) in DMF (10 ml) was added HOST (0.96 g, 6.26 mmol) at room temperature, followed by the addition of piperidine (0.42 g, 5.01 mmol). The reaction mixture was cooled to 0° C. and to this were added EDC (1.20 g, 6.26 mmol) and triethylamine (2.11 g, 2.91 ml, 20.86 mmol). The reaction mixture was stirred at room temperature for 15 hr and the progress of reaction was monitored by TLC. The reaction mixture was concentrated under reduced pressure. The residue so obtained was taken in ethyl acetate (50 ml) and washed with saturated sodium bicarbonate solution (1×40 ml), brine (1×20 ml) and organic layers separated were dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure to get a crude product. The crude product was purified by column chromatography over silica gel (100-200 mesh) using 40% ethyl acetate in hexanes as an eluent to obtain the title compound (0.41 g, 32.4%). MS: m/z 308 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-57bb51c4eadf4fc49d345108a092d48b
Source noteuspto-grants-2016_07