Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231979Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 70351445, compound

https://huagongshe.com/reaction/231979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCarbamic acid, N-(4,6-dimethoxy-2-pyrimidinyl)-, phenyl esterHCID 10945667—
ReactantHCID 20030418HCID 20030418—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 70351445HCID 7035144570.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

By the procedure of Example 4, 0.4 g of the product of Example 7 was reacted with 0.52 g of phenyl(4,6-dimethoxypyrimidin-2-yl)carbamate and 0.26 g of "DBU" in 10 ml of p-dioxane. After stirring at 25° C. for two hours, the resulting suspension was diluted with about 50 ml of water, and filtered; the resulting filtrate was acidified with concentrated hydrochloric acid to pH 4, then filtered. The residue was washed 2×10 ml water, suction-dried 16 hours, then triturated with about 10 ml of warm ethyl acetate to yield 0.5 g of the subject compound; m.p. 219°-220° C. IR(nujol): 1690 cm-1 (c=o); NMR(CDCl3): ppm 3.9(S, 6H, OCH3); 5.8(S, 1H, py H); 6.0(S, 2H, CH2); 7.9 and 8.2(2S, 2H, tri 2H); 7.1-7.6(m, 4H, Ar+NH); 8.15(m, 1H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851030
Source datasetuspto-grants-1989_07
ORD IDord-c2c3c017f0264fada18f5b647e3c46b0
Source noteuspto-grants-1989_07