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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923984Generated: November 2, 2026

Carbon Disulfide → HCID 59367272, compound

https://huagongshe.com/reaction/1923984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantBenzyl N-(2-aminoethyl)carbamateHCID 2794257—
SolventEthanolHCID 702—
ProductHCID 59367272HCID 5936727289.3%

Reaction Steps

To a suspension of benzyl 2-aminoethylcarbamate LIX (3 g; 15.45 mmol) in anhydrous ethanol (20 mL) was added carbon disulfide (0.47 mL; 7.73 mmol). The mixture was heated under gently reflux for 22 h. After cooling to r.t., the product precipitated and was filtered, washed with anhydrous ethanol (3×) and air dried. Benzyl N-(2-{[(2-{[(benzyloxy)carbonyl]amino}ethyl)carbamothioyl]amino}ethyl)carbamate LX was obtained as white solid (2.97 g; 6.90 mmol; 89.3% yield). 1H NMR (DMSO-d6) 3.10-3.14 (m, 4H), 3.37-3.42 (m, 4H), 5.00 (s, 4H), 7.30-7.37 (m, 12H), 7.54 (brs, 2H); ESIMS found for C21H26N4O4S m/z 431.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178490B2
Source datasetuspto-grants-2012_05
ORD IDord-0c897b4037a24c7cba3989e1a8142de4
Source noteuspto-grants-2012_05