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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606438Generated: November 2, 2026

Pyridine → 4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one

https://huagongshe.com/reaction/1606438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChlorosuccinimideHCID 31398—
Reactant1,3,4,9-tetrahydro-4-methyl-10H-thieno[3,4-b] [1,5]benzodiazepin-10-oneHCID 12521632—
SolventWaterHCID 962—
Product4,9-Dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-oneHCID 12521642—

Reaction Steps

To a suspension of 3.8 g. of 1,3,4,9-tetrahydro-4-methyl-10H-thieno[3,4-b] [1,5]benzodiazepin-10-one in 15 ml. of dry pyridine is added, in portions, a total of 2.18 g. of N-chlorosuccinimide. The resulting solution is heated on a steam bath for 15 minutes, cooled and diluted with water. The solid is collected and recrystallized from methanol, to give a tan solid, m.p. 224°-225°C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953430
Source datasetuspto-grants-1976_04
ORD IDord-06fd8ecebd77456d8fff6bb7f3ab5c15
Source noteuspto-grants-1976_04