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HRID 216965作成日:2026年10月27日
Sodium Carbonate → (S)-tert-Butyl 4-(1-amino-3-(4'-(morpholinosulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate
https://huagongshe.com/reaction/216965
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 4-[(4-Bromobenzene)sulfonyl]morpholine | HCID 253128 | — |
| 反応物 | (S)-tert-Butyl 4-(1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate | HCID 59568592 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (S)-tert-Butyl 4-(1-amino-3-(4'-(morpholinosulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate | HCID 59568573 | 80.5% |
反応手順
(S)-tert-Butyl 4-(1-amino-1-oxo-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 16, step (i), 250 mg) in acetonitrile (8 mL) with 4-(4-bromophenylsulfonyl)morpholine (148 mg) was treated with aqueous sodium carbonate (2M, 0.5 mL) and nitrogen was bubbled through the mixture. 1,1 bis(Di-tert-butylphosphino)ferrocene palladium dichloride (5 mg) was added and the mixture was heated at 85° C. for 18 h under nitrogen. The reaction mixture was evaporated onto silica and purified by chromatography on silica eluting with ethyl acetate/isohexane (50:50 to 100:0) to afford the sub-titled compound (240 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08193239B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-1a89f85327c742928b7a8c64219f76c9 |
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| 出典メモ | uspto-grants-2012_06 |
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