Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753180Generated: November 1, 2026

Ammonia → HCID 67370525, compound

https://huagongshe.com/reaction/1753180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86657086HCID 86657086—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
ProductHCID 67370525HCID 6737052523%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7-azido-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one (50 mg, 0.116 mmol) in DMF (2.5 mL) at 0° C. was added ethynyl-trimethyl-silane (33 μL, 0.23 mmol) followed by ethyl-diisopropyl-amine (24 μL, 0.14 mmol) and copper iodide (11 mg) and the mixture was stirred at 0° C. After one hour the reaction was complete (monitored by LCMS). A saturated aqueous solution of NH4Cl containing a drop of ammonia was added and the mixture extracted with EtOAc (3 times). The organics were washed with brine, dried (Na2SO4), filtrated and concentrated in vacuo. The resulting material was purified by flash chromatography (Biotage SP4, gradient 50-100% EtOAc in hexanes 10 CV; hold 100% EtOAc 7CV) to give 10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-7-[4-(trimethylsilyl)-1H-1,2,3-triazol-1-yl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]-pyrazin-5-one (14 mg, yield: 23%). ESI-MI m/z [M+H]+ 532.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163029B2
Source datasetuspto-grants-2015_10
ORD IDord-ddd59033480c465ab1028ce4387432d2
Source noteuspto-grants-2015_10