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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044707Generated: October 28, 2026

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

https://huagongshe.com/reaction/1044707

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 numberUS08563723B2
Source datasetuspto-grants-2013_10
ORD IDord-8d566d0522734c5b883544ca1130514d
Source noteuspto-grants-2013_10