Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38601Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(3,4-Dichlorophenyl)-7-{(2E)-4-[4-(pyrrolidin-1-ylcarbonyl)piperazin-1-yl]but-2-enoyl}-5,6,7,8-tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/38601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
ReactantPiperazin-1-yl-pyrrolidin-1-yl-methanoneHCID 2760443—
Reactant4-Bromocrotonic acidHCID 6436411—
Reactant(3,4-Dichloro-phenyl)-(5,6,7,8-tetrahydro-9-thia-1,3,7-triaza-fluoren-4-yl)-amineHCID 58116912—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(3,4-Dichlorophenyl)-7-{(2E)-4-[4-(pyrrolidin-1-ylcarbonyl)piperazin-1-yl]but-2-enoyl}-5,6,7,8-tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-amineHCID 5811684110%

Reaction Steps

(2E)-4-Bromobut-2-enoic acid (106 mg, 0.64 mmol) and piperazin-1-yl(pyrrolidin-1-yl)methanone (125 mg, 0.68 mmol) were dissolved in DCM (5.0 mL), and DIPEA (111 mg, 0.85 mmol) was added. The mixture was stirred at rt for 2 h. Subsequently, the compound from Example 15A (150 mg, 0.43 mmol), DIPEA (55 mg, 0.43 mmol) and EDCI (82 mg, 0.43 mmol) were added. The reaction was stirred at 50° C. overnight. Then, water was added, and the mixture was extracted three times with DCM. The combined organic layers were dried over sodium sulfate. The solvent was removed in vacuo, and the residue was purified by preparative HPLC to yield 25 mg (10%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524722B2
Source datasetuspto-grants-2013_09
ORD IDord-907f815ae1db4702b9a88f10da798df7
Source noteuspto-grants-2013_09