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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485464Generated: October 31, 2026

Acetohydrazide → 8-methoxy-1,4-dimethyl-5,6-dihydro-4H-pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepine

https://huagongshe.com/reaction/1485464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
Reactant7-methoxy-3-methyl-4,5-dihydro-1H-pyrido[2,3-b][1,4]diazepine-2(3H)-thioneHCID 86718507—
Solvent1-ButanolHCID 263—
Product8-methoxy-1,4-dimethyl-5,6-dihydro-4H-pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepineHCID 7097987761%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 7-methoxy-3-methyl-4,5-dihydro-1H-pyrido[2,3-b][1,4]diazepine-2(3H)-thione (1.8 g, 8.06 mmol) in n-butanol (25 mL) was added acetohydrazide (5.97 g, 80.61 mmol). The mixture was stirred at 130° C. for 3 hours. The reaction mixture was concentrated in vacuo and washed with brine (20 mL), and then the mixture was filtered through a celite pad. The filtrate was extracted with acetic ester (20 mL×3). The combined organic phase was dried by anhydrous sodium sulphate, and then filtered. The filtrate was concentrated and purified by column chromatograph silica gel (elute: dichloro methane/Methanol: 80:1→35:1→20:1) to give 8-methoxy-1,4-dimethyl-5,6-dihydro-4H-pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepine (1.2 g, 61%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422292B2
Source datasetuspto-grants-2016_08
ORD IDord-2911005f861f44a0993a2dca05b9e45b
Source noteuspto-grants-2016_08