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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821890Generated: November 1, 2026

HCID 11042299, compound → HCID 136365981, compound

https://huagongshe.com/reaction/1821890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11042299HCID 11042299—
Reactanttert-butyl N-(2-(aminooxy)ethyl)carbamateHCID 15610443—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 136365981HCID 13636598189%

Reaction Steps

tert-Butyl 2-[[[phenyl(1H-pyrrolo[2,3-c]pyridin-3-yl)methylene]amino]oxy]ethylcarbamate (429.2 mg, 89%) was prepared as a white foam using phenyl(1H-pyrrolo[2,3-c]pyridin-3-yl)methanone (Reference Example 8) and tert-butyl[2-(aminooxy)ethyl]carbamate following the procedure described for Example 104: Rf 0.42 (90:10 methylene chloride/methanol); 1H NMR (300 MHz, CD3OD) δ1.38-1.39 (9H, s), 3.40-3.44 (2H, m), 3.17-3.20 (1H, t, J=5.7 Hz), 3.26-3.28 (1H, t, J=5.3 Hz), 6.50-6.80 (1H, m), 7.30-7.50 (5H, m), 7.86-8.32 (2H, m), 8.76 (1H, s); ESI MS m/z 381 [C21H24N4O3+H]+; HPLC (Method A) 96.8% (AUC), tR=17.7 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608627B2
Source datasetuspto-grants-2009_10
ORD IDord-16a7c9aa69374ce1899b9d2bb489c76b
Source noteuspto-grants-2009_10