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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453548Generated: October 30, 2026

Methanol → HCID 11553747, compound

https://huagongshe.com/reaction/1453548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 68974497HCID 68974497—
SolventDichloromethaneHCID 6344—
ProductHCID 11553747HCID 11553747—

Reaction Steps

40 μl iodotrimethylsilane are added to a solution of 130 mg (S)-2-[(2-benzyloxycarbonylamino-prop-1-yl)amino]-3-(2-butyn-1-yl)-5-[(4-methyl-quinazolin-2-yl)methyl]-3,5-dihydro-imidazo[4,5-d]pyridazin-4-one in 3 ml dichloromethane. After stirring at ambient temperature for 1 and 3 h, a further 100 μl of iodotrimethylsilane are added on each occasion. The solution is stirred for a further 4 h at ambient temperature and then combined with 5 ml of methanol and evaporated down. Then 1 M hydrochloric acid is added and the aqueous phase is washed twice with dichloromethane. The aqueous phase is made alkaline with sodium carbonate and extracted three times with dichloromethane. The organic extracts are dried over sodium sulphate, the solvent is removed and the residue is purified through silica gel (dichloromethane/methanol 1:0->3:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476671B2
Source datasetuspto-grants-2009_01
ORD IDord-45a7d64c659449f0959804383636792e
Source noteuspto-grants-2009_01