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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605915Generated: November 3, 2026

Pyridine → HCID 12521646, compound

https://huagongshe.com/reaction/1605915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 20355327HCID 20355327—
ReactantHCID 20355348HCID 20355348—
SolventWaterHCID 962—
ProductHCID 12521646HCID 12521646—

Reaction Steps

To a suspension of 0.53g. of the mixture of 7 -chloro-4-methyl-1,3,4,9-tetrahydro-10H-thieno[3,4-b] [1,5] benzodiazepin-10-one and 6-chloro-9-methyl-1,3,4,9-tetrahydro-10H-thieno[3,4-b] [1,5] benzodiazepin-10-one (prepared as described in Example 17) in 5 ml. of dry pyridine is added, in portions, 0.27 g. of N-chlorosuccinimide. The resulting solution is heated on a steam bath for 15-20 minutes, cooled, diluted with water and filtered. The solid is recrystallized from methanol to give a yellow solid which consists of the single isomer of the title, m.p. 244°-246°C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03951981
Source datasetuspto-grants-1976_04
ORD IDord-c2c0beeb6a4a412e906b191049350076
Source noteuspto-grants-1976_04