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HRID 128653생성일: 2026년 10월 24일

8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride → SC-51322

https://huagongshe.com/ko/reaction/128653

반응식

참여 물질

역할이름HCID투입량
반응물8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chlorideHCID 14975983—
반응물8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazideHCID 14975985—
반응물3-[(2-Furanylmethyl)thio]propanoic acid, hydrazideHCID 63580095—
생성물SC-51322HCID 9933831—

반응 단계

8-chlorodibenz[b,f][1,41oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylmethyl)thio]-1-oxopropyl]hydrazide (13) was prepared in the manner 8-chlorodibenz[b,f]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide (6) was prepared, as described above in Example 6, from 3-[(2-furanylmethyl)thio]propanoic acid, hydrazide (12), prepared as described above in Example 12, and 8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carbonyl chloride (2), prepared as described above in Example 2, on a 10 mmol scale. The yield was quantitative. Analysis calculated for C22H20N3O4SCl (M.W. 457.94): C, 57.70; H, 4.40; N, 9.18; Cl, 7.74; S, 7.00. Found: C, 57.59; H, 4.36; N, 9.01; Cl, 7.95; S, 7.07.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464830
출처 데이터셋uspto-grants-1995_11
ORD IDord-49200922f7c94b7b8d05ad8d2df8cf6e
출처 메모uspto-grants-1995_11