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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895982Generated: October 27, 2026

8-amino-5H-benzo[b][1,4]benzoxazepin-6-one → HCID 178465553, compound

https://huagongshe.com/reaction/895982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-amino-5H-benzo[b][1,4]benzoxazepin-6-oneHCID 2756399—
Reactant2-Naphthylmethyl ethanimidothioate hydrobromideHCID 22138705—
SolventEthanolHCID 702—
ProductHCID 178465553HCID 178465553—

Reaction Steps

To a stirred solution of 2-amino-10H-dibenzo[b,f][1,4]oxazepin-11-one (Example 4, 50 mg, 0.22 mmol) in 4 mL of ethanol at 0° C. was added thioacetimidic acid naphthalen-2-ylmethyl ester hydrobromide (65 mg, 0.22 mmol). The reaction was warmed to room temperature overnight. The mixture was concentrated at reduced pressure and partitioned between water (5 mL) and ethyl acetate (25 mL). The aqueous layer was separated and evaporated under vacuum (yield 70 mg, 92%). H1 NMR (DMSO d6) δ: 11.15 (bs, 1H), 10.68 (s, 1H), 9.44 (bs, 1H), 8.56 (bs, 1H), 7.71-7.70 (m, 1H), 7.54-7.53 (m, 2H), 7.40-7.36 (m, 1H), 7.20-7.17 (m, 3H), 2.31 (s, 3H), MS (ES): MH+ 268.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919328B1
Source datasetuspto-grants-2005_07
ORD IDord-d1e932c3f07547b5934f1964769a7d45
Source noteuspto-grants-2005_07