Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 90102638 | HCID 90102638 | — |
| Solvent | Triethyl phosphite | HCID 31215 | — |
| Product | HCID 90102936 | HCID 90102936 | 48% |
Reaction Steps
A solution of {4-[(E)-2-(4-iodo-2-methoxy-pyridin-3-yl)-vinyl]-2-methoxy-5-nitro-phenyl}-carbamic acid tert-butyl ester (560 mg, 1.06 mmol) in triethyl phosphite (5.0 ml) was refluxed for 3 h, cooled to 25° C. and poured into water. The aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried over magnesium sulfate. Filtration followed by concentration in vacuo gave a brown solid. Flash chromatography (70/30 hexanes/ethyl acetate) afforded [2-(4-iodo-2-methoxy-pyridin-3-yl)-5-methoxy-1H-indol-6-yl]-carbamic acid tert-butyl ester (250 mg, 48%) as a white solid. MH+ 496.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388166B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-327c1021f1a34adc8f16332eb1bc752c |
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| Source note | uspto-grants-2016_07 |
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