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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80463생성일: 2026년 10월 24일

Veratrylamine → 1,1-Dimethylethyl 4-[{4-(benzyloxy)-2-[(3,4-dimethoxybenzyl)carbamoyl]phenyl}(isobutoxycarbonyl)amino]piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/80463

반응식

참여 물질

역할이름HCID투입량
반응물VeratrylamineHCID 79832—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물SodiumHCID 5360545—
반응물5-(Benzyloxy)-2-({1-[(1,1-dimethylethoxy)carbonyl]piperidin-4-yl}[(2-methylpropoxy)carbonyl]amino)benzoic acidHCID 59587117—
용매DimethylformamideHCID 6228—
생성물1,1-Dimethylethyl 4-[{4-(benzyloxy)-2-[(3,4-dimethoxybenzyl)carbamoyl]phenyl}(isobutoxycarbonyl)amino]piperidine-1-carboxylateHCID 66603782—

반응 단계

A mixture of 6 g of sodium salt of 5-(benzyloxy)-2-({1-[(1,1-dimethylethoxy)carbonyl]piperidin-4-yl}[(2-methylpropoxy)carbonyl]amino)benzoic acid obtained in stage 1.3 and 4.42 g of DIEA in 250 ml of DMF is stirred at AT for 15 min. 6.48 g of HBTU are added and the mixture is left stirring for 30 min. 2.48 g of veratrylamine are added and the reaction mixture is stirred for 48 h 00. It is evaporated under reduced pressure, the residue is taken up in AcOEt, washed with a saturated NH4Cl solution and with a saturated NaHCO3 solution, dried over Na2SO4 and filtered, and the solvent is evaporated under reduced pressure. The residue is chromatographed on silica gel, elution being carried out with an AcOEt/heptane mixture, (20/80, v/v) as far as (60/40, v/v), to give 7.5 g of expected product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846654B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ef7fdc0c79504a6f83b11d3ddad648fd
출처 메모uspto-grants-2014_09