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HRID 265216作成日:2026年10月27日

Hydrochloric Acid → N-Acetylthyroxine

https://huagongshe.com/reaction/265216

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Acetic AnhydrideHCID 7918—
反応物Levothyroxine SodiumHCID 23666112—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Sodium HydroxideHCID 14798—
溶媒Ammonium HydroxideHCID 14923—
生成物N-AcetylthyroxineHCID 2063838090%

反応手順

L-Thyroxine sodium salt, pentahydrate (1) (10 g, 11 mmol) was nearly completely dissolved in 400 mL of ETCH/2N NH4OH (1/1, v/v), filtered, and filtrate poured into 425 mL of 5% HCl. The resulting precipitate was isolated by vacuum filtration and dried under high vacuum to afford a white solid. This material was dissolved in 160 mL DMF, 100 mL (1.06 mol) of acetic anhydride added, and reaction stirred for 1.5 hours, then diluted with 850 mL H2O and allowed to stand at 4° C. for 16 hours. The resulting precipitate was isolated by filtration, then dissolved in 350 mL EtCH and 41 mL of 1N NaOH, stirred for 2.5 hours, 680 mL of 5% HCl added, and mixture allowed to stand at 4° C. for 16 hours. The resulting precipitate was isolated by vacuum filtration and dried under high vacuum to yield 8.1 g (90%) of the desired N-acetyl L-thyroxine (5) as a white solid; 1H NMR (200 MHz, CD3OD) d 7.8 (s, 2H), 7.1 (s, 2H), 4.6-4.7 (m, 1H), 2.8-3.0 (m, 2H), 2.0 (s, 3H); mass spec (FAB) (M+H)+820.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05648272
出典データセットuspto-grants-1997_07
ORD IDord-2f053ae5761b40eca8afc9aa31317f8c
出典メモuspto-grants-1997_07