Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518997Generated: October 31, 2026

Dichloromethane → HCID 86727352, compound

https://huagongshe.com/reaction/518997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant(Prop-1-en-2-yl)boronic acidHCID 10855372—
ReactantHCID 86727349HCID 86727349—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86727352HCID 86727352328.2%

Reaction Steps

A mixture of 3-(7-bromo-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yloxy)-azetidine-1-carboxylic acid tert-butyl ester (Example #65, Step G, 0.030 g, 0.064 mmol), isopropenyl boronic acid (0.032 g, 0.193 mmol), K2CO3 (0.018 g, 0.13 mmol) and Pd(dppf)Cl2.CH2Cl2 (0.011 g, 0.013 mmol) in dioxane (3 mL) and H2O (0.5 mL) was stirred at 80° C. for 15 h. The mixture was cooled to ambient temperature and the solvent was removed in vacuo. The residue was purified by preparative TLC (eluting with 20% EtOAc in petroleum ether) to give 3-(7-isopropenyl-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yloxy)-azetidine-1-carboxylic acid tert-butyl ester as a white solid (0.09 g, 33%). LC/MS (Table 1, Method 2) Rt=1.241 min.; MS m/z: 429 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-e91c0a37a2874e33b2cfa9948331db82
Source noteuspto-grants-2015_08