Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178017Generated: October 31, 2026

1-Hydroxybenzotriazole → Biphenyl-4-carboxylicacid {2-[4-(3-methyl-thiophene-2-carbonyl)-piperazin-1-yl]-2-oxo-ethyl}-amide

https://huagongshe.com/reaction/1178017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Methyl-2-thenoic acidHCID 90269—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactantbiphenyl-4-carboxylic acid (2-oxo-2-piperazin-1-yl-ethyl)-amide TFA saltHCID 131728551—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBiphenyl-4-carboxylicacid {2-[4-(3-methyl-thiophene-2-carbonyl)-piperazin-1-yl]-2-oxo-ethyl}-amideHCID 6695345972.9%

Reaction Steps

DIPEA (110.8 mg, 0.147 mL, 0.85 mmol) was added to a stirred solution of biphenyl-4-carboxylic acid (2-oxo-2-piperazin-1-yl-ethyl)-amide TFA salt (100 mg, 0.22 mmol) in DMF (3 mL). HOBT (28.3 mg, 0.2 mmol) and EDCI.HCl (91.25 mg, 0.47 mmol) were then added. After 2 minutes 3-methyl-thiophene-2-carboxylic acid (27 mg, 0.19 mmol) was added and the resulting mixture was stirred overnight. The reaction mixture was diluted with cold water. The product was extracted with ethyl acetate and the ethyl acetate layer was washed with NaHCO3 solution, saturated brine solution, dried over sodium sulphate and concentrated under reduced pressure to afford 62 mg (72.9% yield) of biphenyl-4-carboxylicacid {2-[4-(3-methyl-thiophene-2-carbonyl)-piperazin-1-yl]-2-oxo-ethyl}-amide. LC-MS purity: 90.22%, HPLC Purity: 92.38%, 1H NMR: (CDCl3) δ 7.9 (d, 2H), 7.75-7.6 (m, 4H), 7.5 (m, 2H), 7.4 (m, 1H), 7.3-7.4 (m, 2H), 6.9 (d, 1H), 4.3 (d, 2H), 3.7 (m, 6H), 3.5 (m, 2H), 2.4 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-f366abfac90a45b8a7be27b6ae9c0e42
Source noteuspto-grants-2010_11