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HRID 1011617作成日:2026年10月27日

Water → N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methyl)-4-(trifluoromethyl)benzene-sulfonamide

https://huagongshe.com/reaction/1011617

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium borohydrideHCID 4311764—
反応物N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamideHCID 67313312—
溶媒MethanolHCID 887—
生成物N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methyl)-4-(trifluoromethyl)benzene-sulfonamideHCID 5765975437%

反応手順

N-((3-Iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methylene)-4-(trifluoromethyl)benzenesulfonamide (41) (7.41 g, 15.66 mmol) was suspended in MeOH (20 mL). NaBH4 was added portionwise and the reaction was stirred for 3 hr until TLC monitoring revealed the disappearance of starting material. Water (20 mL) was added and MeOH was removed in vacuo. The residue was taken up in EtOAc (100 mL) and washed with sat. aq. NaHCO3 (100 mL) and dried over Na2SO4. The reaction was concentrated in vacuo. The resulting crude product was purified by column chromatography using EtOAc/hexane gradients to yield N-((3-iodo-1-(methoxymethyl)-1H-pyrazol-4-yl)methyl)-4-(trifluoromethyl)benzenesulfonamide (42) (1.44 g, 37% over two steps) as a clear oil that solidified upon standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977368B2
出典データセットuspto-grants-2011_07
ORD IDord-79f24434c5fd493c98a3bf0fc310f1ad
出典メモuspto-grants-2011_07