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HRID 1060963作成日:2026年10月25日

tert-Butanol → N-benzyloxycarbonyl-5-aminomethyl-4-(4-pyridyl)-3-(4-fluorophenyl)pyrazole

https://huagongshe.com/reaction/1060963

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物TetrahydrofuranHCID 8028—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物N-benzyloxycarbonyl-glycyl-N-hydroxysuccinimideHCID 22037183—
反応物1,1-dimethylethyl 4-[5-(4-fluorophenyl)-4-(4-pyridinyl)-1H-pyrazol-3-yl]-1-piperazinecarboxylateHCID 22037321—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物N-benzyloxycarbonyl-5-aminomethyl-4-(4-pyridyl)-3-(4-fluorophenyl)pyrazoleHCID 69409299—

反応手順

A 3 L round bottom flask fitted with a mechanical stirrer, N2 inlet and an addition funnel was was charged with 557 mL (0.56 mol) of 1 M t-BuOK in THF and 53 mL (0.56 mol) of t-BuOH. The ketone, 1 (60 g, 0.28 mol) was dissolved in 600 mL of THF and added to the stirred mixture at room temperature. A yellow precipitate formed and the mixture was stirred for 1 h. N-benzyloxycarbonyl-glycinyl N-hydroxysuccinimide (128.6 g, 0.42 mol) was dissolved in 600 mL of THF and added dropwise at r.t. over 1 h. The mixture was stirred for another 5 minutes and 150 mL of water was added. The pH was adjusted to 6.7 with 70 mL of AcOH. Hydrazine monohydrate (41 mL in 100 mL of water) was added via an addition funnel. The mixture was stirred for 1 h and was diluted with 500 mL of water and 500 mL of ethyl acetate. The biphasic mixture was transferred to a sep funnel and the layers were separated. The aqueous layer was extracted with EtOAc (3×300 mL). The organic layer was dried (Na2SO4), filtered and evaporated to leave 157 g of a crude reddish oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06525059B1
出典データセットuspto-grants-2003_02
ORD IDord-0e3ff7702baa4c17a60bac9f0e2537bd
出典メモuspto-grants-2003_02