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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485432Generated: October 31, 2026

8-Bromo-1-methyl-5,6-dihydrospiro[benzo[b][1,2,4]triazolo[4,3-d][1,4]diazepine-4,1'-cyclopropane] → 1-Methyl-5,6-dihydrospiro[benzo[b][1,2,4]triazolo[4,3-d][1,4]diazepine-4,1'-cyclopropane]

https://huagongshe.com/reaction/1485432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Bromo-1-methyl-5,6-dihydrospiro[benzo[b][1,2,4]triazolo[4,3-d][1,4]diazepine-4,1'-cyclopropane]HCID 70979043—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-Methyl-5,6-dihydrospiro[benzo[b][1,2,4]triazolo[4,3-d][1,4]diazepine-4,1'-cyclopropane]HCID 7100359691%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 8-bromo-1-methyl-5,6-dihydrospiro[benzo[b][1,2,4]triazolo[4,3-d][1,4]diazepine-4,1′-cyclopropane] (150 mg, 0.49 mmol) and palladium on carbon (40 mg) in methanol (10 mL) was stirred for 2 hours at 40° C. under hydrogen atmosphere. The solid was filtered and the filtrate was concentrated to give crude 1-methyl-5,6-dihydrospiro[benzo[b][1,2,4]triazolo[4,3-d][1,4]diazepine-4,1′-cyclopropane] (100 mg, 91%) as yellow oil, used for the next step without further purification. LRMS (M+H+)+: calcd 226.12. found 226.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422292B2
Source datasetuspto-grants-2016_08
ORD IDord-a343e8254d5645eeb1e36633a9f12360
Source noteuspto-grants-2016_08