Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 22627183 | HCID 22627183 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22627322 | HCID 22627322 | — |
Reaction Steps
To a stirred solution of 6-amino-1-(2-chlorobenzyl)-3-isobutyryl-2-propylindole (100 mg) in chloroform (2 ml) was added methylisocyanate (0.5 ml) at 0° C. The reaction mixture was stirred at 20° C. for 1 hour, then evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:1) to give crystals which were recrystallized from a mixture of ethyl acetate and hexane to give 1-(2-chlorobenzyl)-3-isobutyryl-6-(3-methylureido)-2-propylindole (75 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06069156 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-7b21a6b930f84f41a905d82e19a271c5 |
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| Source note | uspto-grants-2000_05 |
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