Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533774Generated: October 29, 2026

Cyclobutanecarbonyl chloride → HCID 46843818, compound

https://huagongshe.com/reaction/533774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanecarbonyl chlorideHCID 78705—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66677984HCID 66677984—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 46843818HCID 4684381830%

Reaction Steps

(5-Chloro-benzo[1,3]dioxol-4-yl)-(6,7,8,9-tetrahydro-5H-dipyrido[2,3-b;3′,4′-d]pyrrol-4-yl)-amine (100 mg, 0.29 mmol) and DIEA (0.15 mL, 0.88 mmol) were dissolved in 1,2-dichloroethane (2 mL) and stirred at room temperature. Cyclobutanecarbonyl chloride (0.04 mL, 0.35 mmol) was added dropwise, and the reaction was stirred for 1 h at room temperature. The reaction was concentrated. The crude material was dissolved in DMSO (3 mL) and filtered. The filtrate was purified directly via prep-LC-MS to provide 69 (37 mg, 30% yield) as a white fluffy solid. LC-MS (M+H=425, obsd.=425).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853391B2
Source datasetuspto-grants-2014_10
ORD IDord-66a9e4fe303f4f3588b9a034e5f290cd
Source noteuspto-grants-2014_10