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HRID 1846749作成日:2026年10月26日
Diisopropylethylamine → 2-((1R,2S)-2-aminocyclohexylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide
https://huagongshe.com/reaction/1846749
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide | HCID 57472013 | — |
| 反応物 | butyl (1S,2R)-2-aminocyclohexylcarbamate | HCID 57472014 | — |
| 生成物 | 2-((1R,2S)-2-aminocyclohexylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide | HCID 57472011 | 22.1% |
反応手順
To a solid of 2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (100 mg, 0.25 mmol) in vial was added ten butyl (1S,2R)-2-aminocyclohexylcarbamate (0.3 M solution in NMP, 1.25 mL, 0.375 mmol) and DIPEA (0.09 mL, 0.5 mmol). It was heated at 80° C. for 2 h, cooled and purified by preparative HPLC to give 2-((1R,2S)-2-aminocyclohexylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (21 mg). MS found for C20H25N2O as (M+H)+ 380.4. UV: λ=219.2, 241.6, 336.7.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08952027B2 |
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| 出典データセット | uspto-grants-2015_02 |
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| ORD ID | ord-33408eb028864036919deeccac002dd7 |
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| 出典メモ | uspto-grants-2015_02 |
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