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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768776Generated: October 27, 2026

8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride → 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(2-thienylmethoxy)acetyl]hydrazide

https://huagongshe.com/reaction/1768776

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chlorideHCID 14975983—
Reactant2-(2-Thienylmethoxy)acetic acid, hydrazideHCID 21744782—
Product8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(2-thienylmethoxy)acetyl]hydrazideHCID 86748364—

Reaction Steps

8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(2-thienylmethoxy)acetyl]hydrazide (21) was prepared in the manner described in Example 6 from 1 mmol of 2-(2-thienyl-methoxy)acetic acid, hydrazide (20), prepared as described above in Example 20, and 1.0 mmol of 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carbonyl chloride (2), prepared as described above in Example 2, to yield 0.28 g (64%) of product. Analysis calculated for C21H18N3O4SCl (M.W. 443.91): C, 56.82; H, 4.09; N, 9.47. Found: C, 56.55; H, 4.08; N, 9.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378840
Source datasetuspto-grants-1995_01
ORD IDord-ab9083c485df47bdb3197e946d3e0d79
Source noteuspto-grants-1995_01