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HRID 1701642作成日:2026年10月27日

Isoproterenone hydrochloride → 3-Hydroxy-4-(2-chloro-3-methoxy-4-methylbenzoyloxy)phenyl isopropylaminomethyl ketone

https://huagongshe.com/reaction/1701642

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2-Chloro-3-methoxy-4-methylbenzoyl chlorideHCID 20535393—
生成物3-Hydroxy-4-(2-chloro-3-methoxy-4-methylbenzoyloxy)phenyl isopropylaminomethyl ketoneHCID 20535380—

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 2-chloro-3-methoxy-4-methylbenzoyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(2-chloro-3-methoxy-4-methylbenzoyloxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with hydrochloric acid there is obtained the hydrochloride salt. When this hydrochloride is catalytically hydrogenated, using a procedure similar to that described above in Example 2B, there is obtained 3-hydroxy-4-(2-chloro-3-methoxy-4-methylbenzoyloxy)-alpha-(isopropylaminomethyl)benzyl alcohol hydrochloride.

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-f039010060cf4a86a2d324d859093ff6
出典メモuspto-grants-1980_03