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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948418Generated: October 31, 2026

Triethylamine → HCID 86761268, compound

https://huagongshe.com/reaction/1948418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
Reactant4-[2-(Acetylamino)-4-methyl-1,3-thiazol-5-yl]-5-bromothiophene-2-sulfonylchlorideHCID 86623146—
SolventDichloromethaneHCID 6344—
ProductHCID 86761268HCID 8676126868%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-[2-(acetylamino)-4-methyl-1,3-thiazol-5-yl]-5-bromothiophene-2-sulfonyl chloride, prepared as in Step III of Example 23 (200 mg; 0.48 mmol; 1 eq), is dissolved in anhydrous DCM (10 ml). The reaction mixture is cooled down to 0° C. and put under nitrogen. Triethylamine (0.4 ml; 2.88 mmol; 6 eq) and 2-piperidin-1-yl-ethylamine (0.16 ml; 1.16 mmol; 2.4 eq) are added successively and the reaction mixture is stirred at 0° C. for 2 hours. The mixture is washed with water, NaHCO3 and dried over MgSO4, affording the title compound (170 mg; 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399497B2
Source datasetuspto-grants-2013_03
ORD IDord-aae52331dc2a4498b2fb37c524366c9a
Source noteuspto-grants-2013_03