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HRID 265230作成日:2026年10月27日

Diisopropylethylamine → 4-(Phenylmethyl) hydrogen L-aspartate

https://huagongshe.com/reaction/265230

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物N2-((tert-Butoxy)carbonyl)-L-asparagineHCID 82035—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物N-tert-Butoxycarbonyl-L-aspartic acid beta-benzyl esterHCID 1581888—
反応物DCCI HOBtHCID 21712060—
反応物PhCH2CH2CO-N-Me-Val-Ile-Asn-Asp(OBzl)-OHHCID 131720093—
反応物HCID 178445939HCID 178445939—
溶媒DimethylformamideHCID 6228—
生成物4-(Phenylmethyl) hydrogen L-aspartateHCID 101186—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05648337
出典データセットuspto-grants-1997_07
ORD IDord-4f09e8f9afa64e4aaf4f7659cdf77203
出典メモuspto-grants-1997_07