関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pentafluorophenyl Trifluoroacetate | HCID 4327891 | — |
| 反応物 | 5-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]pyridine-2-carboxylic acid | HCID 135848307 | — |
| 生成物 | Pentafluorophenyl pyridine-2-carboxylate | HCID 2754830 | — |
反応手順
Using analogous procedures to those described in Example 12, 5-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]pyridine-2-carboxylic acid was reacted with pentafluorophenyl trifluoroacetate to give the pentafluorophenyl pyridine-2-carboxylate which was in turn reacted with diethyl L-glutamate to give diethyl N-{5-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]pyridyl-2-carbonyl}-L-glutamate in 93% yield which was in turn hydrolysed with aqueous sodium hydroxide solution to give N-{5-[N-((6RS)-2-methyl-4-oxo-3,4,7,8-tetrahydro-6H-cyclopenta[g]quinazolin-6-yl)-N-(prop-2-ynyl)amino]pyridyl-2-carbonyl}-L-glutamic acid in 77% yield, m.p. 199°-201° C.;
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05789417 |
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| 出典データセット | uspto-grants-1998_08 |
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| ORD ID | ord-4380aa0e2b2c428bbcb86bcdc55a47ff |
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| 出典メモ | uspto-grants-1998_08 |
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