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HRID 1701641作成日:2026年10月26日

Isoproterenone hydrochloride → 3-Hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketone

https://huagongshe.com/reaction/1701641

反応式

関与物質

役割名称HCID仕込み量
反応物Isoproterenone hydrochlorideHCID 2830496—
反応物o-Propionamidobenzoyl chlorideHCID 20535449—
生成物3-Hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketoneHCID 20535334—

反応手順

Following the procedure described above in Example 58A but using 3,4-dihydroxyphenyl isopropylaminomethyl ketone hydrochloride instead of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride and o-propionamidobenzoyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(o-propionamidobenzoyloxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with methanesulfonic acid there is obtained the methanesulfonate salt. When this methanesulfonate is catalytically hydrogenated, using a procedure similar to that described above in Example 2B, there is obtained 3-hydroxy-4-(o-propionamidobenzoyloxy)-alpha-(isopropylaminomethyl)benzyl alcohol and methanesulfonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE030241
出典データセットuspto-grants-1980_03
ORD IDord-443f724e5496481bb85b2a13f9ecf7ef
出典メモuspto-grants-1980_03