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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262208Generated: November 3, 2026

6-Amino-3,3-dimethyl-1,3-dihydro-2H-indol-2-one → HCID 66712661, compound

https://huagongshe.com/reaction/1262208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Amino-3,3-dimethyl-1,3-dihydro-2H-indol-2-oneHCID 13589229—
ReactantHCID 66712241HCID 66712241—
ProductHCID 66712661HCID 66712661—

Reaction Steps

N-{3-[2-(3,3-Dimethyl-2-oxo-2,3-dihydro-1H-indol-6-ylamino)-pyrrolo[2,1-f][1,2,4]triazin-7-yl]-benzyl}-N-methyl-methanesulfonamide was prepared from N-[3-(2-methanesulfinyl-pyrrolo[2,1-f][1,2,4]triazin-7-yl)-benzyl]-N-methyl-methanesulfonamide and 6-amino-3,3-dimethyl-1,3-dihydro-indol-2-one in an analogous manner to Example 1049. Product isolated as a yellow foam (23 mg, 19%). LCMS (m/e) 491 (M+H), 1H-NMR (CDCl3, 400 MHz) δ 8.73 (s, 1H), 8.11 (d, 1H, J=8.0 Hz), 8.09 (s, 1H), 7.56-7.52 (m, 1H), 7.52-7.46 (m, 1H), 7.44 (s, 1H), 7.35 (d, 1H, J=7.6 Hz), 7.10 (d, 1H, J=8.0 Hz), 7.05-6.98 (m, 2H), 6.93 (s, 1H), 6.86 (d, 1H, J=4.8 Hz), 4.41 (s, 2H), 2.90 (s, 3H), 2.83 (s, 3H), 1.40 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-07018c488f20467d915e34194af1e0b7
Source noteuspto-grants-2013_06