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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974520Generated: October 31, 2026

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

https://huagongshe.com/reaction/1974520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chlorideHCID 14975983—
ReactantN-(methylsulfonyl)-L-phenylalanine, hydrazideHCID 131718326—
Product8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acidHCID 21983467—

Reaction Steps

8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2,[2-[(methylsulfonyl)amino]-1-oxo-3-phenyl]hydrazide (15) was prepared in the manner described above in Example 5 on a 0.51 mmol scale starting with N-(methylsulfonyl)-L-phenylalanine, hydrazide (14), prepared as described above in Example 14, and 8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carbonyl chloride (2), prepared as described above in Example 2, to yield 0.11 g (42%) of product. Analysis calculated for C24H23N4O5SCl (M.W. 514.98): C, 55.98; H, 4.50; N, 10.88; Cl, 6.88. Found: C, 55.81 H, 4.46; N, 10.66; Cl, 6.96.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283240
Source datasetuspto-grants-1994_02
ORD IDord-c236f636fe25478b9b845c7944938b29
Source noteuspto-grants-1994_02