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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793647Generated: November 3, 2026

Triphosgene → HCID 20356910, compound

https://huagongshe.com/reaction/1793647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantIsocyanateHCID 105034—
Reactant3-(Methylsulfonyl)aniline hydrochlorideHCID 2735179—
ReactantHCID 22022835HCID 22022835—
SolventDichloromethaneHCID 6344—
ProductHCID 20356910HCID 2035691055%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of triphosgene (0.22 g, 0.33 eq.) in CH2Cl2 was added 3-methane-sulfonyl-phenylamine hydrochloride (0.5 g, 2.4 mmol), followed by the dropwise addition of TEA (0.37 ml, 1.1 eq.). The mixture was heated to 40° C. for 30 min. It was allowed to cool to rt and stirred for an additional 45 min. The isocyanate solution was then added to a solution of 2-[3-(4-chlorobenzyl)-8-aza-bicyclo[3.2.1]oct-8-yl]-1-methyl-ethylamine (0.18 g, 0.6 mmol) (prepared according to the procedure described in example 4, steps 1 to 4) in 6 ml of CH2Cl2. The mixture was stirred overnight at rt. It was diluted with CH2Cl2 and the organic layer was washed with Na2CO3 (sat.) twice, NaCl (sat.) and dried over Na2SO4. The crude mixture was purified on a silica-gel column with 1% iPrNH2, 9% MeOH in EtOAc to give 55% of Example 5 (M+: 490).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081531B2
Source datasetuspto-grants-2006_07
ORD IDord-23f198ef4e9e47f1a2a8dd10acbcbbba
Source noteuspto-grants-2006_07