Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzene, 1-(6-bromohexyl)-4-methoxy- | HCID 10588171 | — |
| Reactant | 5-Benzyloxy-4-methoxymethyl-betacarboline-3-carboxylic acid isopropyl ester | HCID 54138590 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67595562 | HCID 67595562 | 55.5% |
Reaction Steps
10 mg of an 80% suspension of sodium hydride in oil is mixed with 10 ml of tetrahydrofuran and to 0° C. 404.5 mg of 5-benzyloxy-4-methoxymethyl-9H-pyrido[3,4-b]indole-3-carboxylic acid-(1-methylethyl)-ester is added to the suspension, it is stirred for 10 minutes at 0° C., mixed with 406 mg of 6-(4-methoxyphenyl)-hexyl bromide, and the reaction mixture is stirred for 16 hours at room temperature. After the reaction mixture is worked up as described, 330 mg of 5-benzyloxy-4-methoxymethyl-9-[6-(4-methoxyphenyl)-hexyl]-9H-pyrido[3,4-b]indole-3-carboxylic acid-(1-methylethyl)-ester is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05880126 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-e8861342bc314422b24c718bbbb0fb21 |
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| Source note | uspto-grants-1999_03 |
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