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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527701Generated: October 30, 2026

Triphosgene → HCID 57410463, compound

https://huagongshe.com/reaction/527701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantCyclohexane ethylacetateHCID 21867204—
ReactantHCID 67966824HCID 67966824—
SolventDichloromethaneHCID 6344—
ProductHCID 57410463HCID 5741046381.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-methyl-N1-{6-[(1a-methyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromen-7-yl)oxy]-3-pyridinyl}alaninamide (Intermediate 129, 100 mg) in dry dichloromethane (10 ml) TEA (0.177 ml, 1.273 mmol) was added and the reaction mixture was cooled to 0° C. At this point a solution of triphosgene (37.8 mg, 0.127 mmol) in dry dichloromethane (2.5 ml) was slowly added (over 30 minutes) and the reaction mixture was stirred for 1 hour at the same temperature. The reaction was then quenched with water and the two phases were separated. The organic layer was dried over sodium sulphate, filtered and evaporated and the residue was purified by silica gel chromatography (Companion system, with a gradient from cyclohexane/ethyl acetate 8:2 to cyclohexane/ethyl acetate 1:1) to give the title compound as a white solid (40 mg, 0.103 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346790B2
Source datasetuspto-grants-2016_05
ORD IDord-e7b2b277ad794ea28284bb753a0c9650
Source noteuspto-grants-2016_05