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1,3,3-Trimethyl-2-methyleneindoline → 1,3,3-Trimethyl-6'-morpholinospiro[indoline-2,3'-[3H]-naphtho[2,1-b]pyran]
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,3,3-Trimethyl-2-methyleneindoline | HCID 8351 | — |
| 反応物 | Ethyl orthoformate | HCID 31214 | — |
| 反応物 | 4-Morpholino-2-naphthol | HCID 10988042 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1,3,3-Trimethyl-6'-morpholinospiro[indoline-2,3'-[3H]-naphtho[2,1-b]pyran] | HCID 15868837 | 34% |
反応手順
A mixture of 4-morpholino-2-naphthol (0.47 g;0.002 mol), prepared as in 2(b) above, 1,3,3-trimethyl-2-methyleneindole (0.8 g;0.0022 mol) and triethylorthoformate (10.0 ml) was stirred under nitrogen and heated to reflux for 18 hrs. The resulting purple solution was cooled and evaporated to remove the excess triethylorthoformate and the residue flash chromatographed over silica (40% diethyl ether in hexane) to yield an orange gum (0.28 g; yield 34%). Trituration of the gum with diethyl ether afforded the 1,3,3-trimethyl-6'-morpholinospiro [indoline-2,3'-[3H]-naphtho[2,1-b]pyran having the structure shown below as a pale brown solid, m.pt 191°-194° C. ##STR20##
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05623005 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-65b5dd14fecf47bd973f6544bcddcf9c |
| 出典メモ | uspto-grants-1997_04 |