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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77436Generated: October 30, 2026

Hydrazine hydrate (1:1) → 2-Bromo-4-methyl-4,6-dihydro-5H-thieno[2',3':4,5]pyrrolo[2,3-d]pyridazin-5-one

https://huagongshe.com/reaction/77436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantEthyl 2-bromo-6-formyl-4H-thieno[3,2-b]pyrrole-5-carboxylateHCID 58386865—
ReactantEthyl 2-bromo-6-formyl-4-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylateHCID 58386867—
SolventGlycol monoethyl etherHCID 8076—
Product2-Bromo-4-methyl-4,6-dihydro-5H-thieno[2',3':4,5]pyrrolo[2,3-d]pyridazin-5-oneHCID 5838686194%

Reaction Steps

The N-methylated product 63 (420 mg, 1.33 mmol) was dissolved in warm 2-ethoxyethanol (26 mL). To a refluxed solution of hydrazine monohydrate (1 mL, 31.9 mmol) and 2-ethoxyethanol (5 mL) under nitrogen was added prepared N-methylated product 62 solution dropwise over a 2 hr period and the solution continued to reflux for additional 1 hr. After cooling to room temperature, about half of the 2-ethoxyethanol was removed under reduced pressure and the remaining solution was refrigerated at −20° C. overnight. The precipitate was filtered and washed with 2-ethoxyethanol to give desired pyridazinone 64 (354 mg, 94%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841305B2
Source datasetuspto-grants-2014_09
ORD IDord-3542f092514543c1a04d6cefc50e1ee3
Source noteuspto-grants-2014_09