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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877821Generated: October 30, 2026

Trimethylsilyl iodide → HCID 68291496, compound

https://huagongshe.com/reaction/877821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 68350400HCID 68350400—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 68291496HCID 68291496135.1%

Reaction Steps

A solution of (3R,4S)-benzyl 3-((6-bromo-3-carbamoylpyrrolo[1,2-b]pyridazin-4-yl)amino)-4-methoxypyrrolidine-1-carboxylate (300 mg, 0.61 mmol) in acetonitrile (5 mL), was added iodotrimethylsilane (123 mg, 0.614 mmol) at 0° C., the mixture was then stirred at rt for 2 h. The mixture was diluted with ether (30 mL), stirred for 1 h, filtered and rinsed with ether to give the hydroiodide salt of 6-bromo-4-(((3R,4S)-4-methoxypyrrolidin-3-yl)amino)pyrrolo[1,2-b]pyridazine-3-carboxamide (292 mg, 99% yield) as a brown solid. 1H NMR (400 MHz, METHANOL-d4) δ 8.17 (s, 1H), 7.70 (d, J=1.5 Hz, 1H), 7.07 (s, 1H), 4.97-4.88 (m, 2H), 4.56 (br. s., 1H), 4.16-4.09 (m, 1H), 3.67 (dd, J=11.4, 7.7 Hz, 1H), 3.53-3.50 (m, 3H), 3.50-3.45 (m, 1H), 3.40-3.34 (m, 1H), 3.11 (dd, J=11.6, 8.5 Hz, 1H); MS (ES+) m/z: 353.1, 354.0 (M+H); LC retention time: 2.01 min (analytical HPLC Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987268B2
Source datasetuspto-grants-2015_03
ORD IDord-5104f59f12f642ec9e400bec5a94e760
Source noteuspto-grants-2015_03