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HRID 1900582作成日:2026年10月26日

8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acid → 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylmethyl)amino]-1-oxopropyl]hydrazide

https://huagongshe.com/reaction/1900582

反応式

関与物質

役割名称HCID仕込み量
反応物8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acidHCID 21983467—
反応物8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[[(1,1-dimethylethoxy)carbonyl](2-furanylmethyl)amino]-1-oxopropyl]hydrazideHCID 86748365—
生成物8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylmethyl)amino]-1-oxopropyl]hydrazideHCID 86748366—

反応手順

8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylmethyl)amino]-1-oxopropyl]hydrazide (25) was prepared in the same manner as 8-chlorodibenz-[b,f][1,4]-oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-[(2-thienylmethyl)amino]propylhydrazide, monohydrochloride (18), as described above in Example 18, on a 0.37 mmol scale from 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[[(1,1-dimethylethoxy)carbonyl](2-furanylmethyl)amino]-1-oxopropyl]hydrazide (24), prepared as described above in Example 24, to yield 0.14 g (78%) of product. Analysis calculated for C22H21N4O4Cl. HCl 0.25 H2O (M.W. 481.86): C, 54.84; H, 4.71; N, 11.63. Found: C, 54.56; H, 4.60; N, 11.33.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05576315
出典データセットuspto-grants-1996_11
ORD IDord-53d34c6a0a054da3aceeb3cf697a3f5a
出典メモuspto-grants-1996_11