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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40584생성일: 2026년 10월 24일

2-Naphthalenecarboxaldehyde → 4-Naphthalen-2-ylmethyl-piperazine-1-carboxylic acid phenylamide

https://huagongshe.com/ko/reaction/40584

반응식

참여 물질

역할이름HCID투입량
반응물2-NaphthalenecarboxaldehydeHCID 6201—
반응물Potassium HydroxideHCID 14797—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-phenylpiperazine-1-carboxamideHCID 7015289—
용매DichloromethaneHCID 6344—
생성물4-Naphthalen-2-ylmethyl-piperazine-1-carboxylic acid phenylamideHCID 1166735864%

반응 단계

A solution of piperazine-1-carboxylic acid phenylamide (103 mg) and 2-naphthaldehyde (94 mg) in DCM (2 mL) was treated with NaB(OAc)3H (148 mg). After 16 h, the resulting mixture was treated with 10% aq. KOH (2 mL). The aqueous phase was extracted with DCM (2×3 mL). The combined extracts were dried (MgSO4) and concentrated. Chromatography of the residue gave the title compound as a white foam (111 mg). 1H NMR (400 MHz, CDCl3): 7.85-7.80 (m, 3H), 7.74 (s, 1H), 7.52-7.45 (m, 3H), 7.35-7.25 (m, 4H), 7.05-7.00 (m, 1H), 6.37 (br s, 1H), 3.69 (s, 2H), 3.53-3.48 (m, 4H), 2.55-2.49 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530476B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-bb4c30ad2997441bb4dbb53cd7b65c5c
출처 메모uspto-grants-2013_09