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HRID 234824作成日:2026年10月27日

Hydrazine → HCID 178427630、化合物

https://huagongshe.com/reaction/234824

反応式

関与物質

役割名称HCID仕込み量
反応物HydrazineHCID 9321—
反応物DiisopropylethylamineHCID 81531—
反応物N-Boc-2-chloroethylamineHCID 3795708—
反応物9-Fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 10572880—
反応物9-Chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 19974754—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178427630HCID 178427630—

反応手順

(2-N-tert-butoxycarbonylaminoethyl)hydrazine is prepared by reaction of N-t-butoxycarbonyl-2-chloro-ethylamine with hydrazine following a procedure adapted from J. Med. Chem. 7, 493, (1964). Under a nitrogen atmosphere a solution of (2-N-tert-butoxycarbonylaminoethyl)hydrazine (9.2 g) in anhydrous THF (10 mL) is added during 30' to the stirred 9:1 mixture of 9-fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy)benzo [g]isoquinoline-5,10-dione of Preparative Example 15b (3.0 g) in THF (25 mL) containing N,N-diisopropylethylamine (1.38 mL). A slightly exothermic reaction ensues, and the reaction temperature increases from 21° C. to 24° C. After stirring for one hour at room temperature the obtained precipitate is recovered by suction, washed with THF/n-hexane 1/1 (15 mL) and dried at 40° C. under vacuum, to give 2-[2-(N-tert-butoxycarbonylamino)ethyl[-5-(p-toluenesulfonyloxy)iso-quino[8,7,6-cd]indazole-6(2H)-one (1.33 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05596097
出典データセットuspto-grants-1997_01
ORD IDord-d8fd736de86e4c2b8e3db1257e6b8df0
出典メモuspto-grants-1997_01