Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047041Generated: November 1, 2026

N-bromobutanimide → HCID 67494315, compound

https://huagongshe.com/reaction/2047041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 66735928HCID 66735928—
SolventAcetonitrileHCID 6342—
ProductHCID 67494315HCID 67494315—

Reaction Steps

Compound, 5-(4-(methylsulfonyl)phenoxy)-3-(quinolin-3-yl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (150 mg, 0.22 mmol) was dissolved in ACN (10 mL). NBS (40 mg, 0.22 mmol) was added and the mixture was stirred at room temperature for 1 h. After concentration, the residue, 6-bromo-5-(4-(methylsulfonyl)phenoxy)-3-(quinolin-3-yl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine was used in the next step without further purification. HPLC-MS tR=2.66 min (UV254 nm); mass calculated for formula C34H44BrN5O5SSi2 769.2, observed LCMS m/z 770.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591943B2
Source datasetuspto-grants-2013_11
ORD IDord-65312ddc1391415f9f9282f21538ad64
Source noteuspto-grants-2013_11