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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427259생성일: 2026년 10월 24일

Diisopropylethylamine → Boc-Asp(NEt2)-OBzl

https://huagongshe.com/ko/reaction/427259

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물(3S)-4-(benzyloxy)-3-(((tert-butoxy)carbonyl)amino)-4-oxobutanoic acidHCID 7017887—
반응물Diethylammonium chlorideHCID 10197650—
용매DichloromethaneHCID 6344—
용매Ethyl acetate hexaneHCID 21226206—
생성물Boc-Asp(NEt2)-OBzlHCID 1543202789%

반응 단계

BOP (2.20 g, 5.0 mmol) was added under N2 to a cooled (0°) solution of Boc-Asp-OBzl (1.90 g, 4.6 mmol) in CH2Cl2 (50 ml). After 3 min NHEt2.HCl (0.55 g, 5.0 mmol) and DIPEA (2.4 ml, 1.38 mmol) were added. The resultant solution was stirred at 20-22° for 18 h. The solution was washed with 10% aqueous citric acid (2×), 10% aqueous NaHCO3 (2×) and brine (2×). The organic layer was dried (MgSO4) and concentrated to give an oil. After SiO2 chromatography of the oil using hexane-EtOAc (7:3) as the eluent, Boc-Asp(NEt2)-OBzl (1.55 g, 89%) was obtained as an oil. Under a N2 atmosphere, a solution of the latter compound (1.55 g, 4.09 mmol) in MeOH (100 ml) was mixed with 5% Pd/C (155 mg). The mixture was shaken on a Parr apparatus under H2 (50 psi) for 90 min. The mixture was filtered through a 45 m membrane and the filtrate concentrated to give Boc-Asp(NEt2)—OH (1.15 g, 98%) as an oil. The structure of the product was confirmed by NMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313095B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-6cdeafebc7a0486c8cdcc85f2d8bfff2
출처 메모uspto-grants-2001_11