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2-{[1,1-Dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-bis(benzyloxy)acetophenone hydrobromide → 1,1-Dimethyl-2-(2-phenoxyacetamido)ethylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-{[1,1-Dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-bis(benzyloxy)acetophenone hydrobromide | HCID 20446758 | — |
| 反応物 | 2-{[1,1-Dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-dihydroxy acetophenone hydrobromide | HCID 20446802 | — |
| 生成物 | 1,1-Dimethyl-2-(2-phenoxyacetamido)ethylamine | HCID 11806274 | — |
| 生成物 | 3,4-Dibenzyloxyphenacyl bromide | HCID 12681802 | — |
反応手順
The above acetophenone derivative (A) was itself prepared in 85% yield, as a solid m.p. 141°-143° C. by a similar procedure to that described for the equivalent starting material in Example 11, but from 2-{[1,1-dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-bis(benzyloxy)acetophenone hydrobromide. The latter compound was itself obtained in 40% yield as a solid, m.p. 61°-63° C., from N-(2-amino-2-methylpropyl)-2-phenoxyacetamide and 2-bromo-3',4'-bis(benzyloxy)acetophenone using a procedure similar to that in Example 11.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04423070 |
| 出典データセット | uspto-grants-1983_12 |
| ORD ID | ord-ebb36d08f9ca4acd92be7f997a9ed781 |
| 出典メモ | uspto-grants-1983_12 |