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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1680570생성일: 2026년 10월 27일

4-Methylmorpholine → methyl Boc-phenylalanyl-3-amino-1-adamantanecarboxylate

https://huagongshe.com/reaction/1680570

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
반응물Methyl 3-aminoadamantane-1-carboxylate hydrochlorideHCID 2852886—
반응물Methyl 3-aminoadamantane-1-carboxylateHCID 2852887—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물methyl Boc-phenylalanyl-3-amino-1-adamantanecarboxylateHCID 70566312—

반응 조건

온도-50 °C

반응 단계

5.09 Grams of Boc-L-phenylalanine is dissolved in 25 ml of dry dimethylformamide and 2.13 ml of N-methylmorpholine is added. The reaction mixture is cooled to -50° C. and 2.51 ml of isobutylchloroformate is added. The reaction mixture is stirred for 15 minutes, then 1.77 ml of N-methylmorpholine and 3.93 g of methyl 3-amino-1-adamantanecarboxylate hydrochloride are added and the reaction mixture is stirred until all the methyl 3-amino-1-adamantanecarboxylate dissolves then stored for 3 days at 5° C. The reaction mixture is poured into 100 ml of water and extracted twice with 50 ml of ethyl acetate. The ethyl acetate fractions are washed twice with 50 ml of water, 50 ml of a 0.5 solution of potassium bisulfate, 50 ml of water, 50 ml of a 0.5 M solution of potassium bicarbonate, and 50 ml of water then dried over magnesium sulfate. The solvent is removed under reduced pressure, and the residue is dissolved in 150 ml of 10% chloroform in hexane and purified by low pressure chromatography on silica gel using a gradient of 10% to 50% solution of chloroform in hexane as eluent. Removal of the solvent under vacuum gives the product methyl Boc-L-phenylalanyl-3-amino-1-adamantanecarboxylate which is represented by the following formula ##STR23##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04273704
출처 데이터셋uspto-grants-1981_06
ORD IDord-b3e7dd5d90ae4a6aa08835b747db4187
출처 메모uspto-grants-1981_06