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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273977Generated: November 1, 2026

Hydrazine hydrate (1:1) → HCID 178464653, compound

https://huagongshe.com/reaction/2273977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178464651HCID 178464651—
SolventEthanolHCID 702—
ProductHCID 178464653HCID 17846465367%

Reaction Steps

2.51 g N-[(2,3-Diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methylene]-4-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-benzenesulfonamide was taken up in 50 mL EtOH. After addition of 0.70 mL hydrazine hydrate, the mixture was refluxed for 2 h. After cooling to room temperature, the formed precipitate was filtered off. The filtrate was concentrated, and the residue was triturated with DCM. The solids were filtered off, and the filtrate was evaporated to dryness to give 1.20 g (67%) of 4-Aminomethyl-N-[(2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methylene]benzenesulfonamide as a red oil. 1H NMR (400 MHz, CDCl3) δ 1.14 (t, J=7.22 Hz, 3H), 1.59-1.83 (m, 8H), 3.46 (q, 2H), 3.82 (br.s., 2H), 3.92 (br.s., 2H), 6.82 (s, 1H), 7.40 (d, J=8.13 Hz, 2H), 7.88 (d, J=8.13 Hz, 2H) [NH2 & guanidine NH invisible].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126942B2
Source datasetuspto-grants-2015_09
ORD IDord-2364659b0f194c83a2aca7a309d1ea7f
Source noteuspto-grants-2015_09