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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615262Generated: October 31, 2026

Oxindole → HCID 178517069, compound

https://huagongshe.com/reaction/1615262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxindoleHCID 321710—
ReactantHCID 76846386HCID 76846386—
ProductHCID 178517069HCID 17851706916.9%

Reaction Steps

The compound was synthesized according to the method described for Example A1. Oxindole (8 mg, 0.06 mmol) was reacted with 4-chloro-1H-indazole-6-carbaldehyde (11 mg, 0.06 mmol) to give the title compound as an orange solid (3 mg, 13%). 1H NMR (400 MHz, CD3OD) δ 8.21 (s, 1H), 7.87 (s, 1H), 7.82 (s, 1H), 7.59 (d, 1H, J=7.8 Hz), 7.48 (s, 1H), 7.28 (t, 1H, J=7.9 Hz), 6.95 (d, 1H, J=7.7 Hz), 6.90 (t, 1H, J=8.2 Hz); MS ESI [M+H]+, calcd for [C16H10ClN3O+H]+ 296.1; found m/z 296.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765748B2
Source datasetuspto-grants-2014_07
ORD IDord-5c03229ca40142718b0fdc215ded270f
Source noteuspto-grants-2014_07