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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1175생성일: 2026년 10월 23일

Formaldehyde → Nepsilon-dimethylamino-Nalpha-CBZ-O-t-butyl L-lysine

https://huagongshe.com/ko/reaction/1175

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl EsterHCID 11078219—
촉매ZincchlorideHCID 3007855—
용매MethanolHCID 887—
생성물Nepsilon-dimethylamino-Nalpha-CBZ-O-t-butyl L-lysineHCID 22883010—

반응 단계

A mixture consisting of 3.7 (27.2 mmol) of ZnCl2, 3.2 g (53 mmol) of NaCNBH3 and 60 mL of methanol was prepared to which was added a solution of 18 g (51.7 mmol) of the amine 1 in 180 mL of methanol. After cooling to 10°-15° C. 12.4 mL of 37% formaldehyde (165 mmol) was added dropwise over a 2-3 minute period. The reaction was stirred for 1 hour and monitored by silica gel TLC with elution using a 60:10:1(v/v/v/) mixture of chloroform/methanol/concentrated ammonia (solvent A). One hundred milliliters of water was added and the mixture concentrated to a volume of 200 ml. Ethyl acetate (200 mL) was added and the pH raised to 10.5 with 10% NaOH. The ethyl acetate was separated and the pH of the aqueous phase readjusted to 10.5 and extracted with 200 mL of fresh ethyl acetate. The ethyl acetate extracts were combined, washed with NaCl, dried over Na2SO4, filtered and concentrated to yield, after drying overnight under high vacuum, 14.86 g of viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723619
출처 데이터셋uspto-grants-1998_03
ORD IDord-fcbfd11331bc48daad13c3d9090822ab
출처 메모uspto-grants-1998_03