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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623204Generated: November 2, 2026

Trimethylsilyl isocyanate → HCID 86612267, compound

https://huagongshe.com/reaction/1623204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl isocyanateHCID 70696—
ReactantHCID 86612266HCID 86612266—
Catalyst1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventDichloromethaneHCID 6344—
ProductHCID 86612267HCID 8661226798.9%

Reaction Steps

Trimethylsilyl isocyanate (1.62 mL, 12.0 mmol) and 1,8-diazabicyclo[5.4.0]undec-7ene (one drop) were added to a solution of 1-[4-(methoxyamino)butyl]-2-methyl-1H-imidazo[4,5-c]quinolin-4-amine (3.00 g, 10.0 mmol) in dichloromethane (100 mL). The reaction mixture was stirred overnight at room temperature, then concentrated under reduced pressure to afford 4.1 g of crude N-[4-(4-amino-2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N-methoxy-N′-(trimethylsilyl)urea, which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778963B2
Source datasetuspto-grants-2014_07
ORD IDord-5caf6a3ccee54fdabf8cbe215d4edd41
Source noteuspto-grants-2014_07