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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183334Generated: November 1, 2026

2-(Dimethylamino)acetohydrazide → N-[3-(5-{5-[(Dimethylamino)Methyl](1H-1,2,4-Triazol-3-Yl)}(1H-Indazol-3-Yl))Phenyl]-3,3-Dimethylbutanamide

https://huagongshe.com/reaction/2183334

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)acetohydrazideHCID 68319—
ReactantSodium MethoxideHCID 10942334—
ReactantN-{3-[5-(ethoxyiminomethyl)(1H-indazol-3-yl)]phenyl}-3,3-dimethylbutanamide hydrochlorideHCID 86585603—
SolventMethanolHCID 887—
ProductN-[3-(5-{5-[(Dimethylamino)Methyl](1H-1,2,4-Triazol-3-Yl)}(1H-Indazol-3-Yl))Phenyl]-3,3-DimethylbutanamideHCID 22479849—

Reaction Steps

The title compound was prepared according to the procedure described in Example 329 C using N-{3-[5-(ethoxyiminomethyl)(1H-indazol-3-yl)]phenyl}-3,3-dimethylbutanamide hydrochloride (0.360 g, 0.87 mmol), N-amino-2-(dimethylamino)acetamide (0.304 g, 2.60 mmol) and sodium methoxide in methanol (0.398 mL, 4.37 M). The title compound was isolated after purification by preparative HPLC (0.093 g, 25% yield): 1H NMR (CD3OD) δ 8.72 (s, 1H), 8.16 (t, 1H), 8.08 (dt, 1H), 7.75 (dt, 2H), 7.66 (d, 1H), 7.50 (t, 1H), 3.71 (s, 2H), 2.37 (s, 6H), 2.30 (s, 2H), 1.12 (s, 9H); ES-MS (m/z) 432 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-9e8c64d52e324c97b75193616f2671ff
Source noteuspto-grants-2005_05