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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1273018Generated: October 31, 2026

2-(Dimethylamino)acetohydrazide → HCID 178483338, compound

https://huagongshe.com/reaction/1273018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)acetohydrazideHCID 68319—
ReactantSodium MethoxideHCID 10942334—
Reactant(3-[5-(ethoxyiminomethyl)(1H-indazol-3-yl)]phenyl)-N-(2-piperidylethyl)carboxamideHCID 131724925—
SolventMethanolHCID 887—
ProductHCID 178483338HCID 178483338—

Reaction Conditions

Temperature105 °C

Reaction Steps

To a suspension of (3-[5-(ethoxyiminomethyl)(1H-indazol-3-yl)]phenyl)-N-(2-piperidylethyl)carboxamide.3HCl (412 mg, 0.78 mmol) and N-amino-2-(dimethylamino)acetamide (275 mg, 2.35 mmol) in anhydrous methanol (5.0 mL) in a screw-top pressure tube was added sodium methoxide (626 mL of a 25% w/w in methanol). The tube was sealed, heated in a 105° C. oil bath for 48 h and then concentrated to dryness. Purification of the residue by preparatory TLC using 40% ethyl acetate in methanol gave the desired product after precipitation from methanol/ethyl acetate with ethyl ether (12 mg, 3% yield) 1H NMR (DMSO-d6) δ 13.7 (br s, 1H), 8.7 (br s, 2H), 8.4 (s, 1H), 8.1–8.0 (m, 2H), 7.85 (br d, 1H), 7.7–7.6 (m, 2H), 3.6 (s, 2H), 3.5–3.3 (m, 2H), 2.5–2.2 (m, 6H), 2.2 (s, 6H), 1.6–1.3 (m, 6H); ES-MS (m/z) 473 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208513B2
Source datasetuspto-grants-2007_04
ORD IDord-262a73cebcff47ce957caca0ce692fd1
Source noteuspto-grants-2007_04