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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974517Generated: November 1, 2026

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

https://huagongshe.com/reaction/1974517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
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-[(methylsulfonyl)amino]-1-oxopropyl]hydrazideHCID 15237399—

Reaction Steps

8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[-3-[(methylsulfonyl)amino]-1-oxopropyl]hydrazide (11) was prepared from 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-(3-amino-1-oxopropyl)hydrazide, monohydrochloride (9), prepared as described above in Example 9, and methanesulfonyl chloride, in the manner described in Example 10 above on a 2-mmol scale to yield 0.46 g (52%) of product. Analysis calculated for C18H19N4O5ClS (M.W. 438.88): C, 49.26; H, 4.36; N, 12.77. Found: C, 49.05; H, 4.40; N, 12.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283240
Source datasetuspto-grants-1994_02
ORD IDord-30820bf1416a40a7bebb79447c19dd30
Source noteuspto-grants-1994_02