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1,2-Dichloroethane → (e)-3-{1'-Tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-n-(tetrahydro-pyran-2-yloxy)-acrylamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 反応物 | O-(Tetrahydropyran-2-yl)hydroxylamine | HCID 5142091 | — |
| 反応物 | (E)-3-{1'-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid | HCID 52952089 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (e)-3-{1'-Tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-n-(tetrahydro-pyran-2-yloxy)-acrylamide | HCID 87208986 | — |
反応手順
A solution of (E)-3-{1′-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (387 mg, 1 mmol) in DCM (15 ml) was cooled down to 0° C. EDC (383 mg, 2 mmol) and HOBT (135 mg, 1 mmol) were added, and the mixture was stirred at RT for 1 h. NH2OTHP (146 mg, 1.25 mmol) in DCM (1 ml) was added dropwise and the mixture was stirred at RT. After 4 h, the reaction mixture was washed with a saturated NaHCO3 solution and brine, dried over Na2SO4 and concentrated. The crude residue was purified by column chromatography (eluent: DCM/MeOH 98:2) to give (E)-3-{1′-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-N-(tetrahydro-pyran-2-yloxy)-acrylamide
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09115148B2 |
| 出典データセット | uspto-grants-2015_08 |
| ORD ID | ord-6cd46985d0a0472482362a2337b1f2ae |
| 出典メモ | uspto-grants-2015_08 |