HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439396Generated: October 29, 2026
Methyl Isocyanate → HCID 22411430, compound
https://huagongshe.com/reaction/439396
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | Undec-4-ene | HCID 136496 | — |
| Reactant | 7-Hydroxyindole | HCID 2737651 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22411430 | HCID 22411430 | — |
Reaction Steps
3-(N-Cyclopropyl)amino-4-methyl-1,2,3,4-tetrahydrocyclopent b!indol-7-ol (2.2 g) was dissolved in CH2Cl2 (200 ml) with 1,8-diazabicyclo 5.4.0!undec-7-ene (DBU; 0.21 g) and the solution was cooled to 0° C. A solution of methyl isocyanate (0.52 g in 30 ml CH2Cl2) was added slowly to the cooled solution and the reaction was monitored by thin layer chromatography (silica gel, 1:1 hexane/ethyl acetate). After warming to room temperature, the mixture was washed successively with water (2×100 ml), brine (1×100 ml) and again with water (1×100 ml). The organic layer was dried over Na2SO4 and the solvent removed in vacuo. The crude material was recrystallized from acetonitrile. 3-(N-Cyclo-propyl)amino-4-methyl-1,2,3,4-tetrahydrocyclopent b!indol-7-yl methylcarbamate was isolated as light yellow/white plates (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05514700 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-73048c512ac84c2a872ec78174d9a217 |
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| Source note | uspto-grants-1996_05 |
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