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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711164Generated: November 3, 2026

Hydrazine hydrate (1:1) → HCID 86629527, compound

https://huagongshe.com/reaction/1711164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 86629526HCID 86629526—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 86629527HCID 8662952757%

Reaction Steps

To a solution of 1-{1-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-piperidin-4-yl}-3-methoxy-1-thiophen-3-ylmethyl-urea (0.69 g, 1.56 mmol) in EtOH (15 ml) was added hydrazine hydrate (0.49 ml, 15.6 mmol) and the reaction was stirred at rt for 16 h. The reaction mixture was diluted with Et2O (40 ml) to give a white precipitate. The solid was removed via suction filtration and the filtrate was concentrated in vacuo to give a white foam. Purification by column chromatography on silica gel (CH2Cl2:MeOH:NH4OH, 83:15:2, v/v/v) gave 1-[1-(3-amino-propyl)-piperidin-4-yl]-3-methoxy-1-thiophen-3-ylmethyl-urea as a white foam (0.280 g, 57%). 1H NMR (CDCl3) δ 1.60-1.72 (m, 6H), 2.00 (t, 2H, J=9.0 Hz), 2.07 (br s, 3H), 2.39 (t, 2H, J=6.0 Hz), 2.75 (t, 2H, J=6.0 Hz), 2.98 (d, 2H, J=12.0 Hz), 3.65 (s, 3H), 4.25 (m, 1H), 4.29 (s, 2H), 6.95 (d, 1H, J=3.0 Hz), 7.10 (s, 2H), 7.34 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790747B2
Source datasetuspto-grants-2010_09
ORD IDord-58a62bb50ebd4c1ca212dfb6446ab4fc
Source noteuspto-grants-2010_09