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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051882Generated: October 27, 2026

1,2-Dichloroethane → (cis) (4-Bromothiazol-2-yl) (2,6-dimethylmorpholino)methanone

https://huagongshe.com/reaction/1051882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2,6-Dimethylmorpholine, cis-HCID 641500—
Reactant4-Bromo-1,3-thiazole-2-carboxylic acidHCID 15122065—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(cis) (4-Bromothiazol-2-yl) (2,6-dimethylmorpholino)methanoneHCID 11844468869.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-bromothiazole-2-carboxylic acid (prepared according to the procedure given in WO200857336, 1.35 g, 6.49 mmol) in DMF (15 ml) was added HOBT (1.09 g, 7.14 mmol) at room temperature followed by the addition of (2S,6R)-2,6-dimethylmorpholine (0.75 g, 0.8 ml, 6.49 mmol). The reaction mixture was cooled to 0° C. and to this were added EDC (1.86 gm., 9.73 mmol) and triethylamine (2.63 g, 3.62 ml, 26.00 mmol). Mixture was stirred at room temperature for 15 hr. 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 (150 ml) and washed with saturated sodium bicarbonate solution (1×40 ml) followed by brine (1×20 ml). The organic layer separated was dried over anhydrous sodium sulphate, filtered and concentrated at reduced pressure to get a crude product. The crude product was purified by column chromatography over silica gel (100-200 mesh) using 15% ethyl acetate in hexanes as an eluent to obtain the title compound (1.38 g, 69.7%). MS: m/z 306 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-528df6c938e148369efb3eb55c8e3033
Source noteuspto-grants-2016_07