HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1273018Generated: October 31, 2026
2-(Dimethylamino)acetohydrazide → HCID 178483338, compound
https://huagongshe.com/reaction/1273018
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Dimethylamino)acetohydrazide | HCID 68319 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | (3-[5-(ethoxyiminomethyl)(1H-indazol-3-yl)]phenyl)-N-(2-piperidylethyl)carboxamide | HCID 131724925 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178483338 | HCID 178483338 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208513B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-262a73cebcff47ce957caca0ce692fd1 |
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| Source note | uspto-grants-2007_04 |
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