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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566273Generated: October 31, 2026

Sodium Hydroxide → 7-chloro-5-(2-fluoro-phenyl)-3H-thieno[2,3-e][1,4]diazepin-2-ylamine

https://huagongshe.com/reaction/566273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantChlorineHCID 24526—
Reactant5-(2-fluoro-phenyl)-3H-thieno[2,3-e][1,4]diazepin-2-ylamineHCID 21266008—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product7-chloro-5-(2-fluoro-phenyl)-3H-thieno[2,3-e][1,4]diazepin-2-ylamineHCID 21266010—

Reaction Steps

19 g of 5-(2-fluoro-phenyl)-3H-thieno[2,3-e][1,4]diazepin-2-ylamine were dissolved in 730 ml of 5% methanol in dichloromethane, treated while stirring well with 327 g of a 2.8% solution of chlorine gas in 5% methanol in dichloromethane and stirred at room temperature under argon for 5 minutes. Thereafter, the reaction mixture was poured into 600 ml of 0.2N sodium hydroxide solution while cooling with ice and extracted. The dichloromethane extracts were dried with sodium sulphate, filtered and the solvent was evaporated in a vacuum. After two fold boiling of the residue in 5% methanol in dichloromethane and filtration there were obtained 7.4 g of 7-chloro-5-(2-fluoro-phenyl)-3H-thieno[2,3-e][1,4]diazepin-2-ylamine of m.p. 215-217° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174881B1
Source datasetuspto-grants-2001_01
ORD IDord-8836ab4bc7014ac48c683773645a7f18
Source noteuspto-grants-2001_01