HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372379Generated: October 30, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 67755339, compound
https://huagongshe.com/reaction/2372379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | N-Methyl-(7-isopropoxycarbonyl-6-methyl-5,6-dihydropyrrolo[2,1-b]thiazol-3-yl)acetamide | HCID 19903349 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67755339 | HCID 67755339 | 75% |
Reaction Steps
2.0 g of N-methyl-(7-isopropoxycarbonyl-6-methyl-5,6- dihydropyrrolo[2,1-b]thiazol-3-yl)acetamide was dissolved in a solvent mixture of 60 ml of chloroform and 6 ml of methanol. 0.3 g of 1,8-diazabicyclo[5.4.0]-7-undecene was added thereto and the mixture was stirred at 20° C. for 15 hours. The reaction mixture was then washed with 20 ml of 5% aqueous acetic acid, a 0.5% aqueous solution of sodium hydrogencarbonate and a saturated aqueous solution of sodium chloride. The chloroform layer was dried over anhydrous sodium sulfate. After distilling off the chloroform, the obtained crude crystals were recrystallized from ethanol to thereby give 1.5 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098919 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-6ffb081e98734b2ca9c2636d5126888f |
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| Source note | uspto-grants-1992_03 |
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