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HRID 1393843作成日:2026年10月27日

7-Nitroindazole → HCID 178512945、化合物

https://huagongshe.com/reaction/1393843

反応式

関与物質

役割名称HCID仕込み量
反応物7-NitroindazoleHCID 1893—
反応物AminoguanidineHCID 2146—
反応物HCID 178512947HCID 178512947—
反応物HCID 178512970HCID 178512970—
生成物HCID 178512945HCID 178512945—

反応手順

Agmatine sulfate, aminoguanidine, arcaine sulfate, and 7-nitroindazole were purchased from Sigma Chemical Co. (St. Louis, Mo.). Other agmatine analogues were obtained from a variety of sources. A racemic mixture of alpha-vinylargine was synthesized according to the method of Pederson et al. (1993). Compounds CS51, R74, TRV187, TRV162, G3, and RO5 (see FIG. 1) were obtained from and produced using the methods of Carmignani et al. (2001). The synthesis of 3-aminopropylguanidine and trans-4-aminocyclohexylguanidine were synthesized by adding an aqueous solution of cyanamide drop-wise to a boiling solution of 1,3-diaminopropane or trans-1,4-diaminocyclohexane in a concentrated hydrochloric solution. The mixture was refluxed for 1 hour and then an aqueous solution of NaOH was added. The white precipitate was isolated and an 1H NMR spectrum was obtained to confirm the structures. The synthesis of Bis(3-(N-aminomethyl)-aminopropyl)amine is the same as described for 3-aminopropylguanidine and trans-4-aminocyclohexylguanidine except that it uses N-(3-aminopropyl)-1,3-propyldiamine instead of 1,3-diaminopropane or trans-1,4-diaminocyclohexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07347984B2
出典データセットuspto-grants-2008_03
ORD IDord-9b8b1035b73c458995c7f6e4ceefd46f
出典メモuspto-grants-2008_03