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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058506Generated: November 3, 2026

Aziridine → HCID 11290689, compound

https://huagongshe.com/reaction/1058506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAziridineHCID 9033—
ReactantHCID 11404780HCID 11404780—
SolventDichloromethaneHCID 6344—
ProductHCID 11290689HCID 1129068984%

Reaction Steps

A stirred solution of the above amide (315 mg, 0.95 mmol) in CH2Cl2 (35 mL) was treated with aziridine (197 μL, 3.81 mmol) at room temperature for 8 h. The mixture was partitioned between more CH2Cl2 and water, and the organic layer was dried and concentrated under reduced pressure. The residue was dissolved in EtOAc and filtered through a short column of silica gel to give 8 (269 mg, 84%): mp (CH2Cl2/iPr2O) 137° C.; 1H NMR [(CD3)2SO] δ8.86 (t, J=5.6 Hz, 1 H, NH), 8.66 (s, 1H, H-3), 7.40 (s, 1H, H-6), 3.63 (s, 3H, Me), 3.51-3.43 (m, 2H, NHCH2), 2.61 (t, J=6 8 Hz, 2H, CH2CO), 2 48 (s, 4H, aziridine-H). Anal. Calcd for C13H14N4O7: C, 46.15;H, 4 17; N, 16 57. Found: C, 45.89,H, 3.89; N, 16.45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06517836B1
Source datasetuspto-grants-2003_02
ORD IDord-6a6ff077b85a4b75840ba69f52bb6406
Source noteuspto-grants-2003_02