HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187342Generated: October 29, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 11016088, compound
https://huagongshe.com/reaction/2187342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Carbamic acid, N-(4,6-dimethoxy-2-pyrimidinyl)-, phenyl ester | HCID 10945667 | — |
| Reactant | HCID 11108888 | HCID 11108888 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11016088 | HCID 11016088 | — |
Reaction Steps
A suspension of 1.50 g of 5-(2-dimethylamino-1-azaethenyl)-2-methoxycarbonylbenzenesulfonamide, 1.61 g of 4,6-dimethoxy-2-phenoxycarbonylaminopyrimidine, 32 ml of acetonitrile and 0.83 ml of DBU is stirred initially at 0° C. and then at room temperature until the reaction has ended. The reaction mixture is then concentrated under reduced pressure. The residue is taken up in water and washed with diethyl ether. The aqueous phase is carefully acidified with conc. hydrochloric acid (pH 6) and the sulfonylurea precipitate is separated off, washed with diisopropyl ether and water and dried. This affords 1.89 g of the desired sulfonylurea, melting point 73-75° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410482B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-6a4ad6ed00144a1396842a210de12e0f |
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| Source note | uspto-grants-2002_06 |
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