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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974534Generated: October 31, 2026

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

https://huagongshe.com/reaction/1974534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarbonyl chlorideHCID 68242—
Reactant8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-(3-amino-1-oxopropyl)hydrazide, monohydrochlorideHCID 131717719—
Product8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylcarbonyl)amino]-1-oxopropyl]hydrazideHCID 86747546—

Reaction Steps

8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylcarbonyl)amino]-1-oxopropyl]hydrazide (31) was prepared from 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-(3-amino-1-oxopropyl)hydrazide, monohydrochloride (9), prepared in the manner described above in Example 9, and 2-furoyl chloride in the same manner as described in Example 10 on a 1.9 mmol scale to yield 0.37 g (43%) of product. Analysis calculated for C22H19N4O5Cl (M.W. 454.87): C, 49.26; H, 4.36; N, I2.77; Cl, 7.79. Found: C, 49.05; H, 4.40; N, 12.66; cl, 7.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283240
Source datasetuspto-grants-1994_02
ORD IDord-bd8c7c44506a4a0e9fa896090d33bf8c
Source noteuspto-grants-1994_02