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Methylamine tetrahydrofuran → 4-(Methyaminomethyl)phenyloxycarbonyl-glutamic acid di-tert-butyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methylamine tetrahydrofuran | HCID 66615946 | — |
| 反応物 | HCID 87930423 | HCID 87930423 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(Methyaminomethyl)phenyloxycarbonyl-glutamic acid di-tert-butyl ester | HCID 69644845 | 78% |
反応手順
A stirred solution of 40 (6.1 g, 14.9 mmol) in dichloromethane (50 mL) was treated with 2 N methylamine-THF solution (10 mL) at 0° C. overnight. After removal of solvents, the residual oil was dissolved in methanol (80 mL) and placed in an ice-bath. To the above solution was added sodium borohydride in small portions over 30 min. The reaction solution was kept at 0° C. for 1 hour, and solvent was then evaporated. The residue was worked up with brine and dichloromethane. After separation, the organic phase was dried over anhydrous MgSO4, rotary evaporated and dried in vacuum. The crude amine 41 (5.4 g, 78%) was obtained as a light yellow glassy solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06855695B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-581076baa3bd49d7840e6c654d9bdd43 |
| 出典メモ | uspto-grants-2005_02 |