Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl (1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetate hydrochloride | HCID 71552668 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86614346 | HCID 86614346 | — |
Reaction Steps
Step a): To a stirred solution of Intermediate 1 (20 mg, 0.068 mnol) and DIEA (35 μl, 0.20 mmol) in dichloromethane (1 ml) is added phenyl isocyanate (8.2 μl, 0.075 mmol). The reaction mixture is kept stirring at rt for 1 h, then 1N HCl (2 ml) was added. The aqueous layer is extracted twice with dichloromethane. The organic layers are combined and the solvent is evaporated to give crude ethyl (2-phenylcarbamoyl-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetic acid: tR (LC-2) 2.23 min; ESI-MS (positive ion): m/z 400.39 [M+Na]+ (calcd 377.44 for C22H23N3O3); 1H-NMR (CDCl3): 1.19 (t, J=7.0 Hz, 3H); 2.77 (t, J=5.3 Hz, 2H); 3.91 (t, J=5.3 Hz, 2H); 4.14 (q, J=7.0 Hz, 2H); 4.65 (s, 2H); 4.68 (s, 2H); 6.46 (s, 1H); 6.98 (t, J=7.0 Hz, 1H); 7.04-7.09 (m, 1H); 7.14-7.16 (m, 2H); 7.20-7.26 (m, 2H); 7.32-7.35 (m, 2H); 7.40 (d, J=7.6 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714132B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-1526a124ecdd4467a7df569bf1e5f46c |
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| Source note | uspto-grants-2010_05 |
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