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HRID 829作成日:2026年10月24日

Hydrochloric Acid → Methyl 2-[[[[(4-Methoxy-6-methyl-1,3,6-triazin-2-yl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/ja/reaction/829

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1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物Carbamic acid, (4-methoxy-6-methyl-1,3,5-triazin-2-yl)-, phenyl esterHCID 11448329—
反応物Methyl 2-(aminosulfonyl)-1-methyl-1H-pyrrole-3-carboxylateHCID 15790330—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物Methyl 2-[[[[(4-Methoxy-6-methyl-1,3,6-triazin-2-yl)amino]carbonyl]amino]sulfonyl]-1-methyl-1H-pyrrole-3-carboxylateHCID 19693847—

反応手順

Methyl 2-(aminosulfonyl)-1-methyl-1H-pyrrole-3-carboxylate (0.10 g, 0.46 mmol) and 0.13 g (0.50 mmol) of phenyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate were combined in 2 mL of acetonitrile and 0.075 mL of DBU was added and the resulting amber solution was stirred at ambient temperature for 30 min. The reaction mixture was diluted with 15 mL of water and acidified with 0.5 mL 1N HCl and the resulting precipitate was collected by filtration and rinsed successively with water and ether, then dried to afford 0.13 g oil the title compound as a white solid, m.p. 189°-190° C. (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723410
出典データセットuspto-grants-1998_03
ORD IDord-a5a19d2e3ccc4cb7bff13f06f043ffc0
出典メモuspto-grants-1998_03