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L-Glutamic Acid → Glycylglycine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | L-Glutamic Acid | HCID 33032 | — |
| 反応物 | Boc-Trp | HCID 44424848 | — |
| 反応物 | HCID 178454169 | HCID 178454169 | — |
| 生成物 | Glycylglycine | HCID 11163 | — |
反応手順
The synthesis of the peptide resin 15 was done according to the method described in Example 6 by building on Boc glycine resin (2.0 g, 0.3 mmol Gly/g) or by using resin 14a and adding Boc-Trp, Boc-His (Bzl) and Pyro-Glu. Amino acid analysis gave Gly2.0 Ser0.96 Pro1.05 Glu1.05 Leu1.06 Tyr1.13 Arg1.10 BzlHis0.86. A suspension of 1.1 g of 13 in absolute ethanol was photolyzed and purified as described in Example 7. The purified protected decapeptide 15 was obtained in 64% yield (0.257 g): m.p. 155°-159°; tlc Rf1 0.80, Rf2 0.11, Rf3 0.75, Rf4 0.04; UV max (MeOH) 262 mμ (t = 6000); the nmr was consistent with the structure; [α]27D - 22 (c 1 (CH3CO2H); the amino acid composition was Gly1.90 Ser0.92 Pro1.0 Leu1.0 Tyr0.92 Arg1.02 Glu1.02.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04062746 |
| 出典データセット | uspto-grants-1977_12 |
| ORD ID | ord-7f5c948b9b3a45d3933f0ef2cd25ebc9 |
| 出典メモ | uspto-grants-1977_12 |