HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494142Generated: October 29, 2026
Methyl Isocyanate → HCID 68867688, compound
https://huagongshe.com/reaction/494142
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 68865270 | HCID 68865270 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 68867688 | HCID 68867688 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538112B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-9dcbcb1adbc547f2bea9faa3beeb44c4 |
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| Source note | uspto-grants-2009_05 |
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