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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25142Generated: October 28, 2026

Methanol → HCID 178449225, compound

https://huagongshe.com/reaction/25142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11537093HCID 11537093—
Reactantmethyl N-(3,5-diamino-6-chloropyrazine-2-carbonyl)carbamimidothioate;hydroiodideHCID 140329753—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178449225HCID 178449225194%

Reaction Steps

1-(3,5-Diamino-6-chloropyrazinoyl-2-methyl-pseudothiourea hydroiodide (0.32 g, 0.8 mmol) was added to a solution of amine 115 (0.25 g, 1.2 mmol) in a mixture of THF (15 mL), methanol (5 mL) and diisopropylethylamine (1 mL). The reaction mixture was stirred at reflux for 3.5 h and then cooled to room temperature. The formed precipitate was isolated, washed with ethyl acetate (2×5 mL) and treated with 5% HCl (10 mL). The resulting solid was isolated by filtration, washed with water and dried under vacuum to give compound 116 (0.25 g, 73%) as a yellow solid. 1H NMR (300 MHz, DMSO-d6) δ 1.56 (m, 4H), 2.57 (m, 2H), 3.32 (m, 2H), 3.70 (m, 2H), 3.93 (m, 2H), 4.90 (t, 1H), 6.84 (d, 2H), 7.12 (d, 2H), 7.45 (s, 2H), 8.70 (br s, 1H), 8.88 (br s, 1H), 9.12 (br s, 1H) 10.45 (s, 1H). APCI MS m/z=422 [C18H24ClN7O3+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858615B2
Source datasetuspto-grants-2005_02
ORD IDord-c0a070977d2c451284950da28aab1df3
Source noteuspto-grants-2005_02