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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433000Generated: November 4, 2026

4-[3-(4-Tert-butoxycarbonylamino-pyridin-3-yl)-propenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl ester → 1-[3-(4-Amino-pyridin-3-yl)-propenyl]-4-[2-(5-chloro-thiophen-2-yl)-ethenesulfonyl]-piperazin-2-one

https://huagongshe.com/reaction/1433000

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[3-(4-Tert-butoxycarbonylamino-pyridin-3-yl)-propenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl esterHCID 53878143—
Reactant2-(5-Chlorothiophen-2-yl)ethenesulfonyl chlorideHCID 54463064—
SolventAcetonitrileHCID 6342—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product1-[3-(4-Amino-pyridin-3-yl)-propenyl]-4-[2-(5-chloro-thiophen-2-yl)-ethenesulfonyl]-piperazin-2-oneHCID 69028457—

Reaction Steps

4-[3-(4-tert-Butoxycarbonylamino-pyridin-3-yl)-propenyl]-3-oxo-piperazine-1-carboxylic acid tert-butyl ester from EXAMPLE 96, Part B (45 mg, 0.10 mmol) is dissolved in 20% TFA/CH2Cl2 and stirred at r.t. for 2 hours. The solution is concentrated to residue. The residue is dissolved in MeCN (2.5 ml) and treated with 4-methylmorphorline (0.027 ml, 0.25 mmol). 2-(5-Chloro-thiophen-2-yl)-ethenesulfonyl chloride (24 mg, 0.10 mmol), EXAMPLE 3, in MeCN (1 mL) is then added dropwise. The reaction mixture is stirred at r.t. for 1 h, then subjected to reverse phase HPLC purification, to give the title compound as white solid (0.040 g, 0.037 mmol). MS m/z 439, 441 (M+H); 1H NMR (CD3OD, 300 MHz) δ8.20 (br, 1H), 8.10 (s, 1H), 8.08 (d, 1H), 7.60 (d, 1H), 7.53 (d. 1H), 7.35 (d, 1H), 7.21 (d, 1H), 7.07 (d, 1H), 6.82 (d, 1H), 5.27 (m, 1H), 3.88 (s, 2H), 3.60-3.50 (m, 4H), 3.30 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-604b143b7931429387d19ba4afa05d09
Source noteuspto-grants-2009_11