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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072602Generated: November 3, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 14346817, compound

https://huagongshe.com/reaction/2072602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 14179827HCID 14179827—
ReactantHCID 14346816HCID 14346816—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 14346817HCID 1434681779.9%

Reaction Steps

To 0.22 g of 2-(5-methyl-1H-tetrazol-1-yl)benzenesulfonamide (compound of Example 2, 0.32 g) and 0.32 g of phenyl (4,6-dimethoxy-1,3,5-triazin-2-yl)-(methyl)-carbamate in 4 ml of dry acetonitrile was added at room temperature 0.2 ml of DBU. The reaction mixture was allowed to stand for four days, then diluted with 4 ml of water, several ice chips and 4 ml of diethyl ether. After stirring this solution for one minute, the ether layer was removed by pipet and the remaining mixture was acidified by dropwise addition of 1N HCl. The resulting precipitate was filtered, washed with water and dried to give 0.32 g of a white solid, m.p. 180°-182° C. (d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04913726
Source datasetuspto-grants-1990_04
ORD IDord-7fedaee3a31e44cb8de8b9212085e981
Source noteuspto-grants-1990_04