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HRID 1258388作成日:2026年10月27日

N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide → N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1258388

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 67329899—
反応物4,5-dichloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 67330668—
反応物3-mercapto-N-cyclopropylpropanamideHCID 86656567—
生成物N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 6732989937%
生成物N-cyclopropyl-3-(1-oxo-4-(thiophen-2-ylsulfonylimino)-1,4-dihydronaphthalen-2-ylthio)propanamideHCID 67330263—

反応手順

N-cyclopropyl-3-(1-oxo-4-(thiophen-2-ylsulfonylimino)-1,4-dihydronaphthalen-2-ylthio)propanamide (13h) was prepared according to the procedure for 13d except using 4,5-dichloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophenesulfonamide (12c) and 3-mercapto-N-cyclopropylpropanamide ( ), which afforded the title compound 20 mg (37%) as a yellow solid, m.p.: ° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08466157B2
出典データセットuspto-grants-2013_06
ORD IDord-eedfdb1f37fe47db887dfc21ce7702eb
出典メモuspto-grants-2013_06