Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768785Generated: October 26, 2026

4-(Thiophen-3-yl)butanoic acid → 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-4-(3-thienyl)butyl]hydrazide

https://huagongshe.com/reaction/1768785

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Thiophen-3-yl)butanoic acidHCID 11041143—
Reactant8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, hydrazideHCID 13560461—
Product8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-4-(3-thienyl)butyl]hydrazideHCID 15285362—

Reaction Steps

8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-4-(3-thienyl)butyl]hydrazide (33) was prepared in the manner described in Example 7 on a 5.2 mmol scale from 3-thiophenebutanoic acid (32), prepared as described above in Example 32, and 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, hydrazide (1), prepared as described above in Example 1, to yield 0.87 g (37%) product. Analysis calculated for C22H20N3O3SCl (M.W. 441.94): C, 59.79; H, 4.56; N, 9.51; Cl, 8.02. Found: C, 59.76; H, 4.58; N, 9.54; Cl, 8.06; S, 7.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378840
Source datasetuspto-grants-1995_01
ORD IDord-d6fadaa298f443bc90cd0edeb3291713
Source noteuspto-grants-1995_01