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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016227Generated: October 31, 2026

Benzyl succinimido carbonate → HCID 131723617, compound

https://huagongshe.com/reaction/1016227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl succinimido carbonateHCID 83172—
Reactantmethyl N-(3,5-diamino-6-chloropyrazine-2-carbonyl)carbamimidothioate;hydroiodideHCID 140329753—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 131723617HCID 13172361783%

Reaction Steps

1-(3,5-Diamino-6-chloropyrazinoyl)-2-methyl-pseudothiourea hydroiodide (II, 494 mg, 1.27 mmol) was dissolved in a mixture of anhydrous DMF (10 mL), and triethylamine (3 mL) followed by treatment with N-(benzyloxycarbonyloxy) succinimide (470 mg, 1.7 mmol) dissolved in DMF (3 mL). The reaction mixture was stirred overnight at room temperature. After this time, the reaction mixture was concentrated under reduced pressure and the residue suspended in ethyl acetate (30 mL). Silica gel (25 g) was added to the solution and the solvent was evaporated to leave the silica gel impregnated with the crude product that was purified by flash chromatography on a FlashElute™ system from Elution Solution (P.O. Box 5147, Charlottesville, Va. 22905) using a 90 g silica gel cartridge (eluent: hexanes, ethyl acetate=1:2). The purified N-Cbz-1-(3,5-diamino-6-chloropyrazinoyl)-2-methyl-pseudothiourea (III) was obtained as a pale yellow solid: 416 mg (83% yield); 1H NMR (360 MHz, DMSO-d6) δ 2.33 (s, 3H), 2.61 (s, 3H), 4.99 (s, 2H), 7.39 (m, 10H), 13.7 (s, 1H); API MS m/z=395 [C15H15ClN6O3S+H]+; LC/MS (Method A) >99%, tr=10.1 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06475509B1
Source datasetuspto-grants-2002_11
ORD IDord-306cfa95c12648148a62b5f1b9cce418
Source noteuspto-grants-2002_11