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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518995Generated: October 31, 2026

Dichloromethane → HCID 86727350, compound

https://huagongshe.com/reaction/518995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantHCID 86727349HCID 86727349—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86727350HCID 8672735039.8%

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 (0.080 g, 0.17 mmol), cyclopropyl boronic acid (0.044 g, 0.52 mmol), K2CO3 (0.047 g, 0.34 mmol) and Pd(dppf)Cl2.CH2Cl2 (0.014 g, 0.017 mmol) in dioxane (3 mL) and H2O (0.5 mL) was stirred at 100° C. for 15 h. The mixture was cooled to ambient temperature and the solvent was removed in vacuo. The residue was purified by preparative HPLC (Table 3, Method 4) to give 3-(7-cyclopropyl-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 pale yellow solid (0.029 g, 33%). LC/MS (Table 1, Method 2) Rt=1.228 min.; MS m/z: 429 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-5b14fe2e27ac424ab6c5c72877baf310
Source noteuspto-grants-2015_08