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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615232Generated: October 31, 2026

N-(2-Oxoindolin-6-yl)acetamide → HCID 178474027, compound

https://huagongshe.com/reaction/1615232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Oxoindolin-6-yl)acetamideHCID 2749839—
ReactantHCID 178519388HCID 178519388—
ProductHCID 178474027HCID 178474027—

Reaction Steps

The title compound was synthesized according to the method described for Example A11B except substituting N-(2-oxoindolin-6-yl)acetamide (30 mg, 0.158 mmol) and 1H-benzo[d][1,2,3]triazole-6-carbaldehyde (26 mg, 0.174 mmol) to obtain 22 mg, 44%. 1H NMR (400 MHz, d6-DMSO) δ ˜16 (s, 1H), 10.60 (s, 1H), 10.10 (s, 1H), 8.23 (s, 1H), 8.01 (s, 1H), 7.73 (d, J=8.0 Hz, 1H), 7.64 (s, 1H), 7.51 (s, 1H), 7.47 (d, J=8.0 Hz, 1H), 6.86 (d, J=7.4 Hz, 1H), 2.02 (s, 3H); MS ESI 320.1 [M+H]+, calcd for [C17H13N5O2+H]+ 320.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765748B2
Source datasetuspto-grants-2014_07
ORD IDord-4a3673af7fba483c90b8599ad119e0ee
Source noteuspto-grants-2014_07