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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494142Generated: October 29, 2026

Methyl Isocyanate → HCID 68867688, compound

https://huagongshe.com/reaction/494142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
ReactantHCID 68865270HCID 68865270—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 68867688HCID 68867688—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-amino-2-(4-fluorobenzyl)-10-benzyloxy-8-methyl-7,8-dihydropyrazino[1′,2′:1,5]pyrrolo[2,3-d]pyridazine-1,9(2H,6H)-dione (75 mg, 168 μmol) and methylisocyanate (24 mg, 419 μmol) in anhydrous 1,2-dichloroethane (3 mL) was heated in a sealed tube in an oil bath at 100° C. overnight. The product mixture was concentrated under vacuum. The intermediate dicarbonimidic diamide was dissolved in methanol, treated with an aqueous solution of KOH (0.1 mL, 2 M), and stirred at room temperature for one hour, and concentrated under vacuum. The residue was partitioned between chloroform and dilute hydrochloric acid. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum to provide the title compound. ES MS M+1=505

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538112B2
Source datasetuspto-grants-2009_05
ORD IDord-9dcbcb1adbc547f2bea9faa3beeb44c4
Source noteuspto-grants-2009_05