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HRID 10256作成日:2026年10月25日

Ethylene Glycol → 4-Methyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(p-tolyl)-4-pyrimidinyl]-amide

https://huagongshe.com/reaction/10256

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物1,2-DimethoxyethaneHCID 8071—
反応物SodiumHCID 5360545—
反応物4-Methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amideHCID 21979552—
溶媒DimethylformamideHCID 6228—
生成物4-Methyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(p-tolyl)-4-pyrimidinyl]-amideHCID 21979576—

反応手順

To a mixture of 1,2-dimethoxyethan (15 ml) and ethyleneglycol (40 ml) was added sodium (298 mg) in small portions. The mixture was stirred until the sodium was completely dissolved. Then DMF (15 ml), followed by 4-methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide (1.0 g, Referential Example 14) was added. Stirring was continued for 4 days at 100° C. The mixture was evaporated and water (150 ml) was added to the residue followed by addition of acetic acid (1.0 ml). The precipitate was filtered off, washed with water and dried. The crude material was purified by chromatography over silicagel with EtOAc/methanol/aquous ammonia (25%)=4/1/0.5 to give 4-methyl-phenyl sulfamic acid-[6-(2-hydroxy-ethoxy)-5-(p-tolyl)-4-pyrimidinyl]-amide (500 mg). tR=4.38 (LC); [M+H]+=415.19 (ES+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094781B2
出典データセットuspto-grants-2006_08
ORD IDord-542f35727f4d4e29a5f0506e1410f87a
出典メモuspto-grants-2006_08