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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527702Generated: October 30, 2026

Triphosgene → HCID 57410580, compound

https://huagongshe.com/reaction/527702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantHCID 67967035HCID 67967035—
SolventDichloromethaneHCID 6344—
ProductHCID 57410580HCID 57410580129.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N1-[6-(1H-spiro[2-benzopyran-4,1′-cyclopropan]-5-yloxy)-3-pyridinyl]-isovalinamide (Intermediate 141, 40 mg) in dry dichloromethane (8 mL) TEA (0.076 mL, 0.544 mmol) was added and the reaction mixture was cooled to 0° C. A solution of triphosgene (14.54 mg, 0.049 mmol) in dry dichloromethane (4 ml) was slowly added and the reaction mixture was stirred for 3 hours at the same temperature. The reaction was quenched with water (10 ml) and two phases separated. The organic layer was dried over sodium sulphate, filtered and evaporated and the residue was purified by flash chromatography (Biotage system) on silica gel using 10 g SNAP column and cyclohexane/ethyl acetate as eluents from 7:3 to 3:7 as eluent. This afforded the title compound (25 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346790B2
Source datasetuspto-grants-2016_05
ORD IDord-e4d47c5f94214c048097da29fca4c8ab
Source noteuspto-grants-2016_05