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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 867033생성일: 2026년 10월 25일

Dimethylformamide → Nalpha-benzyloxycarbonyl-L-glutaminyl-L-tryptophan methyl ester

https://huagongshe.com/reaction/867033

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물L-Glutamine, N2-[(phenylmethoxy)carbonyl]-HCID 75855—
반응물Diphenylphosphoryl azideHCID 123414—
반응물Methyl tryptophanate hydrochlorideHCID 2734891—
용매TriethylamineHCID 8471—
생성물Nalpha-benzyloxycarbonyl-L-glutaminyl-L-tryptophan methyl esterHCID 54382161—

반응 단계

To a stirred mixture of Nα -benzyloxycarbonyl-L-glutamine, 56 g., and L-tryptophan methyl ester hydrochloride, 56 g., in 300 ml. of dimethylformamide at 5° C. is added diphenylphosphorazidate, 47.5 ml., in 100 ml. of dimethylformamide dropwise over ten minutes followed by 61.6 ml. of triethylamine over one hour. The mixture is stirred in an ice bath for three hours and at room temperature for 18 hours. After evaporation the residue is dissolved in 1 l. of ethyl acetate and washed successively with 500 ml. of 1N hydrogen chloride solution, 500 ml. of a saturated solution of sodium bicarbonate and 500 ml. water. The ethyl acetate layer is separated, dried, evaporated and 74.2 g. of Nα -benzyloxycarbonyl-L-glutaminyl-L-tryptophan methyl ester is obtained by recrystallization from methanol; m.p. 197°-198° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04101538
출처 데이터셋uspto-grants-1978_07
ORD IDord-9376b45e89e64d1881ccf64f84b8f763
출처 메모uspto-grants-1978_07