関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | L-Glutamine, N2-[(phenylmethoxy)carbonyl]- | HCID 75855 | — |
| 反応物 | Diphenylphosphoryl azide | HCID 123414 | — |
| 反応物 | Methyl tryptophanate hydrochloride | HCID 2734891 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | Nalpha-benzyloxycarbonyl-L-glutaminyl-L-tryptophan methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04101538 |
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| 出典データセット | uspto-grants-1978_07 |
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| ORD ID | ord-9376b45e89e64d1881ccf64f84b8f763 |
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| 出典メモ | uspto-grants-1978_07 |
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