Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | HCID 68692459 | HCID 68692459 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68695596 | HCID 68695596 | 60% |
Reaction Steps
A stirred solution of 187 (120 mg, 0.39 mmol) in dry DMF (1.5 mL) was treated at 0° C. with N,N-dimethyl-1,2-ethanediamine (107 μL, 0.97 mmol), followed by the dropwise addition of diethyl cyanophosphonate (128 μL, 93%, 0.78 mmol). The mixture was warmed to room temperature for 45 min, then poured into dilute aqueous NH3 saturated with NaCl. The resulting solid was collected, washed with water and recrystallised twice from CH2Cl2/i-Pr2O to give 1-(chloromethyl)-N-[2-(dimethylamino)ethyl]-5-nitro-1,2-dihydro-3H-benzo[e]indole-8-carboxamide (188) (88 mg, 60%) as a red solid: mp 178-180° C.; 1H NMR [(CD3)2SO] δ 8.68 (t, J=5.7 Hz, 1H), 8.22 (d, J=1.2 Hz, 1H), 8.16 (d, J=9.1 Hz, 1H), 7.77 (dd, J=9.1, 1.7 Hz, 1H), 7.72 (s, 1H), 6.41 (d, J=1.7 Hz, 1H), 4.28-4.18 (m, 1H), 3.98 (dd, J=10.9, 3.7 Hz, 1H), 3.84 (td, J=9.7, 2.4 Hz, 1H), 3.75 (dd, J=−11.0, 9.0 Hz, 2H), 3.49-3.37 (m, 2H), 2.45 (t, J=7.0 Hz, 2H), 2.21 (s, 6H). Anal. (C18H21ClN4O3) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718688B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-b14d10d1f8c0483a98bc27e67523c60c |
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| Source note | uspto-grants-2010_05 |
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