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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162144Generated: November 3, 2026

B-(1E)-1-Hexenylboronic acid → (E)-tert-Butyl 3-(3-(hex-1-enyl)imidazo[1,2-b]pyridazin-6-ylamino)propylcarbamate

https://huagongshe.com/reaction/1162144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantB-(1E)-1-Hexenylboronic acidHCID 5326225—
ReactantDichloromethane methanol ammonium hydroxideHCID 21896990—
Reactanttert-Butyl 3-(3-bromoimidazo[1,2-b]pyridazin-6-ylamino)propylcarbamateHCID 57470631—
Product(E)-tert-Butyl 3-(3-(hex-1-enyl)imidazo[1,2-b]pyridazin-6-ylamino)propylcarbamateHCID 86621015—

Reaction Steps

Prepared from the product from step A and (E)-1-hexeneboronic acid according to general procedure 2 providing the crude Boc-protected olefin (122 mg, 96%) as a brown oil: Rf=0.71 (CH2Cl2/MeOH/NH4OH, 160:18:2); 1H NMR (500 MHz, CD3OD) δ 7.78 (d, J=9.7 Hz, 1H), 7.54 (s, 1H), 6.64-6.40 (m, 3H), 3.47 (q, J=6.3 Hz, 2H), 3.29-3.23 (m, 2H), 2.36-2.30 (m, 2H), 1.84-1.81 (m, 2H), 1.50-1.42 (m, 11H), 1.40-1.48 (m, 2H), 0.93 (t, J=7.3 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820670B2
Source datasetuspto-grants-2010_10
ORD IDord-93dc3da2d77c43cfa215d510e480f9f1
Source noteuspto-grants-2010_10