Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371639Generated: October 28, 2026

Pyridine → HCID 12521646, compound

https://huagongshe.com/reaction/371639

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 0.53 g. 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 numberUS04087421
Source datasetuspto-grants-1978_05
ORD IDord-b3fb5c221f92411caf493762d122cf9c
Source noteuspto-grants-1978_05