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HRID 428476作成日:2026年10月25日

Succinate → tert-Butyl ((2S,4S,5S)-5-(2-(2,6-dimethylphenoxy)acetamido)-4-hydroxy-1,6-diphenylhexan-2-yl)carbamate

https://huagongshe.com/reaction/428476

反応式

関与物質

役割名称HCID仕込み量
反応物SuccinateHCID 160419—
反応物Sodium BicarbonateHCID 516892—
反応物5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane, (2S,3S,5S)-HCID 11997926—
反応物(2,6-Dimethylphenoxy)acetyl ChlorideHCID 12353505—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物tert-Butyl ((2S,4S,5S)-5-(2-(2,6-dimethylphenoxy)acetamido)-4-hydroxy-1,6-diphenylhexan-2-yl)carbamateHCID 45039081—

反応手順

[2S,3S,5S]-2-Amino-3-hydroxy-5-t-butyloxycarbonylamino-1,6-diphenylhexane×0.5 succinate (111.9 g, 0.25 mol) was charged to a 2L, 3-necked round-bottomed flask with mechanical stirring. NaHCO3 (106 g, 1.26 mol), 600 ml H2O and 600 ml EtOAc were added and stirred vigorously until all solids were dissolved (15 minutes). Stirring was slowed and a solution of the 2,6-dimethyl-phenoxyacetyl chloride and EtOAc (100 ml) was added in a narrow stream via addition funnel. After 30 min of stirring, starting materials were consumed (HPLC analysis) and the layers were separated. The aqueous layer was extracted with EtOAc, the organic layers were combined and washed with 200 ml of 1 M NaOH, 200 ml of 10% HCl, 200 ml of brine, dried over MgSO4, filtered and concentrated to provide the desired product as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313296B1
出典データセットuspto-grants-2001_11
ORD IDord-f6fbcc125bdb46f6a3195a811e349b6c
出典メモuspto-grants-2001_11