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HRID 1175作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl EsterHCID 11078219—
触媒ZincchlorideHCID 3007855—
溶媒MethanolHCID 887—
生成物Nepsilon-dimethylamino-Nalpha-CBZ-O-t-butyl L-lysineHCID 22883010—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723619
出典データセットuspto-grants-1998_03
ORD IDord-fcbfd11331bc48daad13c3d9090822ab
出典メモuspto-grants-1998_03