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HRID 412473作成日:2026年10月26日

Acetic Acid → (R)-3-{4-[(4-tert-butylcyclohexylamino)methyl]benzoylamino}-2-hydroxypropionic acid

https://huagongshe.com/reaction/412473

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物4-tert-ButylcyclohexylamineHCID 79396—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物(R)-3-(4-Formylbenzoylamino)-2-hydroxypropionic acidHCID 86586064—
溶媒MethanolHCID 887—
溶媒Trimethyl orthoformateHCID 9005—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(R)-3-{4-[(4-tert-butylcyclohexylamino)methyl]benzoylamino}-2-hydroxypropionic acidHCID 67485259—

反応手順

The above resin bound (R)-3-(4-formylbenzoylamino)-2-hydroxypropionic acid was treated with a 0.5 M solution of 4-tert-butylcyclohexylamine (0.25 mmol) in a mixture of N-methyl-2-pyrrolidinone and trimethylorthoformate (1:1, 0.5 mL) and glacial acetic acid (50 μL) for 1 hour at 25° C. Sodium cyanoborohydride (250 μmol, 16 mg) dissolved in a mixture of N-methyl-2-pyrrolidinone and methanol (1:1, 0.25 mL) was added and the mixture was vortexed at 25° C. for 4 hours followed by filtration and washing with a mixture of N-methyl-2-pyrrolidinone and methanol (1:1, 2×1 mL) 3×1 mL N-methyl-2-pyrrolidinone (3×1 mL) and a mixture of 1,2-dichloropropane and diisopropylethylamine (7:1, 2×0.75 mL).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06562807B2
出典データセットuspto-grants-2003_05
ORD IDord-fa4a1c5ab51e473fb5cb99043408e8c8
出典メモuspto-grants-2003_05