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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396062Generated: November 4, 2026

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

https://huagongshe.com/reaction/1396062

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 numberUS08901108B2
Source datasetuspto-grants-2014_12
ORD IDord-cc2e9f04ea1f42e4a68c7e2d252e3a1d
Source noteuspto-grants-2014_12