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HRID 243594作成日:2026年10月25日

Dimethyl Sulfoxide → HCID 86598720、化合物

https://huagongshe.com/reaction/243594

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Valine methyl esterHCID 94285—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Sodium Acetate TrihydrateHCID 23665404—
反応物Tert-butyl 2-hydroxyethyl[(2-methyl-1,3-thiazol-4-yl)methyl]carbamateHCID 66890987—
溶媒DichloromethaneHCID 6344—
溶媒Methanol--water (1/1)HCID 22242641—
生成物HCID 86598720HCID 86598720—

反応条件

温度0 °C

反応手順

A solution of the product of Example 143B (2.26 g) in dichloromethane (20 mL) was treated with oxalyl chloride (5.4 mL, 1.5 equivalents) at −78° C., and stirred for 15 min. DMSO (1.02 mL, 2 equivalents) was added dropwise at −78° C., stirred for 15 min, and quenched with triethylamine (4 mL, 4 equivalents) as the mixture warmed to 0° C. The mixture was quenched with 20% KH2PO4, and partitioned between dichloromethane and water. The organic layer was washed with brine, dried over Na2SO4, filtered, and the solvents were evaporated. To this crude product was added methanol/water (7:2), (L)-valine methyl ester (1.21 g, 1 equivalent), sodium acetate trihydrate (1.96 g, 2 equivalents), and NaCNBH3 (0.95 g, 2 equivalents) was added portionwise over 30 min. After stirring for 1 hour the mixture was partitioned between saturated NaHCO3 and extracted with ethyl acetate (2×). The combined organic layer was washed with brine, dried with Na2SO4, and evaporated. The residue was treated with dichloromethane/trifluoacetic acid (10 mL, 1:1) and stirred at 25° C. for 2 hrs and concentrated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653141B2
出典データセットuspto-grants-2014_02
ORD IDord-7e087acf65324b1281b990c4c9c01926
出典メモuspto-grants-2014_02