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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199230Generated: October 30, 2026

Triethylamine → HCID 59580673, compound

https://huagongshe.com/reaction/2199230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Methylthio)propionyl ChlorideHCID 12921440—
ReactantHCID 59580961HCID 59580961—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 59580673HCID 5958067381%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of (2,4-dichloro-thiazol-5-yl)-carbamic acid tert-butyl ester (1.0 g, 3.7 mmol) in dichloroethane (20 mL) stirring at room temperature was added triethylamine (935 mg, 9.25 mmol), followed by dropwise addition of methylsulfanyl-propionyl chloride (776 mg, 5.6 mmol) and the mixture was stirred for 5 min before DMAP (45 mg, 0.37 mmol) was added. The mixture was stirred at 75° C. for 4 h. The reaction mixture was cooled, quenched with H2O (30 mL). The organic layer was separated and the aqueous layer extracted with dichloromethane (20 mL). The combined organic layer was dried over Na2SO4 and purified by silica gel chromatography (0 to 100% ethyl acetate/hexanes) to give product as a colorless oil (1.11 g, 81%): 1H NMR (300 MHz, CDCl3) δ 3.32 (t, J=7.3 Hz, 2H), 2.83 (t, J=7.3 Hz, 2H), 2.16 (s, 3H), 1.46 (s, 9H); ESIMS m/z 371.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09357780B2
Source datasetuspto-grants-2016_06
ORD IDord-e9eb1cb72c754a3281714f3c8fcacf3e
Source noteuspto-grants-2016_06