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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444701Generated: October 29, 2026

Isopropylamine → HCID 77492458, compound

https://huagongshe.com/reaction/444701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67116105HCID 67116105—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
ProductHCID 77492458HCID 7749245845.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2Z)-3-(3-bromo-2-thienyl)-2-cyano-3-{[1-(1,3-thiazol-2-yl)ethyl]amino}acrylic acid (0.18 g, 0.468 mmol, 1 eq.) in 5 ml of DCM (CH2Cl2) were added isopropylamine (0.083 g, 1.40 mmol, 3 eq.), hydroxybenzotriazole (HOBT) (0.066 g, 0.49 mmol, 1.05 eq.) and diisopropylethylamine (DIPEA) (0.090 g, 0.70 mmol, 1.5 eq.). The reaction was cooled to 0° C. and dicyclohexylcarbodiimide (DCC) (0.101 g, 0.49 mmol, 1.05 eq.) was added. Stirring was allowed overnight and the solid formed removed by filtration. The solvent was removed under reduced pressure and the residual oil submitted to chromatography on silica gel to give 2Z)-3-(3-bromo-2-thienyl)-2-cyano-N-isopropyl-3-{[1-(1,3-thiazol-2-yl)ethyl]amino}acrylamide (0.090 g, 43% yield) as a white solid and a mixture of atropoisomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476197B2
Source datasetuspto-grants-2013_07
ORD IDord-6a46019ecc1548ddb00deee41cfeafca
Source noteuspto-grants-2013_07