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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590865Generated: October 30, 2026

Pyridine → HCID 118271847, compound

https://huagongshe.com/reaction/590865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantHCID 118271680HCID 118271680—
SolventDichloromethaneHCID 6344—
ProductHCID 118271847HCID 118271847—

Reaction Steps

To an 8 mL vial charged with 2-methoxyacetyl chloride (6.6 mg, 0.061 mmol) was added (R)-1-(3-amino-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea (30 mg, 0.056 mmol) in DCM (1 ml) and pyridine (0.045 ml, 0.557 mmol). The vial was capped and the contents stirred at room temperature for 16 h. The reaction mixture was diluted with DCM (1 mL), MP-Trisamine (137 mg, 0.278 mmol) added, and the contents of the vial shaken at room temperature for 3 h. The resin was filtered, and washed through with DCM (1 mL). The volatiles were removed in vacuo to afford crude (R)-2-methoxy-N-(6-(3-(1-phenylethyl)ureido)-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-yl)acetamide, which was taken forward without purification. MS ESI calc'd. For C37H35N6O3 [M+H]+ 611. found 611.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-c698db372afa4c4294bcc552d195212b
Source noteuspto-grants-2016_01