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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164726Generated: October 26, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-[[(4-Methoxy-6-methyl-2-pyrimidinyl)aminocarbonyl]aminosulfonyl]-N-methoxybenzenecarboximidoyl chloride

https://huagongshe.com/reaction/1164726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantPhenyl (4-methoxy-6-methylpyrimidin-2-yl)carbamateHCID 13577349—
Reactant2-(Aminosulfonyl)-N-methoxybenzenecarboximidoyl chlorideHCID 54018765—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-[[(4-Methoxy-6-methyl-2-pyrimidinyl)aminocarbonyl]aminosulfonyl]-N-methoxybenzenecarboximidoyl chlorideHCID 5378662452.6%

Reaction Steps

To a suspension of 0.4 g of the product of Example 4 and 0.46 g of phenyl(4-methoxy-6-methylpyrimidin-2-yl)carbamate in 10 ml of dry acetonitrile was added 0.25 g of DBU. The suspension was stirred for about two hours at room temperature, then diluted with excess water and filtered. The filtrate was acidified with concentrated hydrochloric acid to yield a precipitate. After filtration, the residue was washed with excess water and suction-dried to yield 0.35 g of the subject compound, m.p. 178° to 179° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906282
Source datasetuspto-grants-1990_03
ORD IDord-7922528f22594bbe8e11c38d22122967
Source noteuspto-grants-1990_03