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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265230생성일: 2026년 10월 27일

Diisopropylethylamine → 4-(Phenylmethyl) hydrogen L-aspartate

https://huagongshe.com/reaction/265230

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물N2-((tert-Butoxy)carbonyl)-L-asparagineHCID 82035—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물N-tert-Butoxycarbonyl-L-aspartic acid beta-benzyl esterHCID 1581888—
반응물DCCI HOBtHCID 21712060—
반응물PhCH2CH2CO-N-Me-Val-Ile-Asn-Asp(OBzl)-OHHCID 131720093—
반응물HCID 178445939HCID 178445939—
용매DimethylformamideHCID 6228—
생성물4-(Phenylmethyl) hydrogen L-aspartateHCID 101186—

반응 단계

A modified procedure of example I was used to assemble the protected tetrapeptide (SEQ ID NO:5) PhCH2CH2CO-N-Me-Val-Ile-Asn-Asp(OBzl)-OH wherein Boc-Asp(OBzl)-OH was linked to the photo-resin and HOBt/DCC was used for coupling Boc-Asn-OH. A solution of the protected tetrapeptide (375 mg, 0.54 mmol) and 3-methyl-1(S)-(5-1H-tetrazolyl)butylamine (375 mg, 1.25 mmol) in DMF (15 ml) was cooled to 0. DIPEA (284 mg) and then diphenylphosphoryl azide (760 mg) were added to the solution. The reaction mixture was stirred for 16 h at 0 and then partitioned between Et2O and H2O containing of few drops of concentrated NH4OH (pH=9.5). The aqueous phase was separated, washed with fresh Et2O and filtered through a 45 m membrane. The pH of the filtrate was adjusted to pH 6.5 by the addition of AcOH and again filtered through a 45 m membrane. The filtrate was loaded on a HPLC preparatory column. The column was eluted with a continuous gradient of 0.06% aqueous TFA in acetonitrile. The pure fractions as indicated by analytical HPLC were combined and lyophilized to give the corresponding Asp(OBzl) protected peptide (132 mg) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648337
출처 데이터셋uspto-grants-1997_07
ORD IDord-4f09e8f9afa64e4aaf4f7659cdf77203
출처 메모uspto-grants-1997_07