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HRID 525036作成日:2026年10月26日
Disodium 2,3-dihydroxybutanedioate → (S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamate
https://huagongshe.com/reaction/525036
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Disodium 2,3-dihydroxybutanedioate | HCID 13355 | — |
| 反応物 | 4-Aminotetrahydropyran | HCID 419223 | — |
| 反応物 | Trimethylaluminum | HCID 16682925 | — |
| 反応物 | (S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylate | HCID 86722033 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamate | HCID 86722055 | — |
反応手順
Tetrahydro-2H-pyran-4-amine (900 microl, 8.69 mmols) was added to a solution of (S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylate (900 mg, 2.89 mmols, preparation 109) in toluene (36 ml). A 2M solution of Trimethyl aluminium in toluene (7 ml, 14.00 mmols) was added and it was stirred at 80° C. overnight. Water (50 ml) and a 0.5M solution of sodium tartrate (25 ml) were added. It was extracted with ethylacetate. The combined organic layers were washed with water and brine. It was dried, filtered and concentrated in vacuum. The title compound was obtained (617 mg, 56%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09340547B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-04de8d8e819c4455b3734c36e5918338 |
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| 出典メモ | uspto-grants-2016_05 |
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