돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49843생성일: 2026년 10월 25일

Oxalyl chloride → N3-(5-Chlorothiophen-2-ylcarbonyl)-N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamine

https://huagongshe.com/reaction/49843

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물5-Chloro-2-thiophenecarboxylic acidHCID 95048—
반응물N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamineHCID 12150690—
용매PyridineHCID 1049—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N3-(5-Chlorothiophen-2-ylcarbonyl)-N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamineHCID 1299057262.3%

반응 단계

A solution of 5-chlorothiophene-2-carboxylic acid (120 mg, 0.72 mmol) in methylene chloride and DMF (0.005 mL) was treated with oxalyl chloride (0.105 mL, 1.20 mmol). After 0.25 h, the mixture was concentrated and the residue was dissolved in chloroform. This solution was added dropwise to a solution of N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamine (170 mg, 0.6 mmol) in pyridine and chloroform. The reaction mixture was then purified using a procedure similar to that described in Example 2, Part D, yielding 160 mg (58%) of the title compound as a hydrochloride salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710057B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-0208a0524ee5473484eeef0ced84e59f
출처 메모uspto-grants-2004_03