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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366066Generated: October 27, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 178429879, compound

https://huagongshe.com/reaction/1366066

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-{5-[4-(4-Bromo-2-fluorophenylamino)-1,5-dimethyl-6-oxo-1,6-dihydro-pyridin-3-yl]-tetrazol-1-yl}-propionitrileHCID 66674434—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178429879HCID 17842987977%

Reaction Steps

DBU (0.030 mL, 0.21 mmol) was added to a solution or 3-{5-[4-(4-bromo-2-fluorophenylamino)-1,5-dimethyl-6-oxo-1,6-dihydro-pyridin-3-yl]-tetrazol-1-yl}-propionitrile (30 mg, 0.069 mmol) in methylene chloride (1.5 mL). After 2 hours, the reaction mixture was diluted with ethyl acetate and washed with 1 N HCl. The aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated under reduced pressure. Trituration with diethyl ether gave clean desired product (20 mg, 77%); MS APCI (−) m/z 377, 379 (M−, Br pattern) detected: 1H NMR (400 MHz, CD3OD) δ 8.20 (s, 1H) 7.29 (dd, 1H), 7.13 (dd, 1H), 6.63 (t, 1H), 3.65 (s, 3H), 1.91 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893065B2
Source datasetuspto-grants-2011_02
ORD IDord-e4c7b42b71d34c7b95c5640c17065209
Source noteuspto-grants-2011_02