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HRID 867033作成日:2026年10月26日

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

https://huagongshe.com/reaction/867033

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物L-Glutamine, N2-[(phenylmethoxy)carbonyl]-HCID 75855—
反応物Diphenylphosphoryl azideHCID 123414—
反応物Methyl tryptophanate hydrochlorideHCID 2734891—
溶媒TriethylamineHCID 8471—
生成物Nalpha-benzyloxycarbonyl-L-glutaminyl-L-tryptophan methyl esterHCID 54382161—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04101538
出典データセットuspto-grants-1978_07
ORD IDord-9376b45e89e64d1881ccf64f84b8f763
出典メモuspto-grants-1978_07