Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | HCID 11961473 | HCID 11961473 | — |
| Product | HCID 22559177 | HCID 22559177 | — |
Reaction Steps
According to the procedure described in the synthesis method of the compound 036 in Example 36 (Preparation Method 5, Step e-1), ethyl 3-(3-bromo-4-hydroxyphenyl)propionate and 1-iodobutane were reacted and treated to obtain ethyl 3-(3-bromo-4-butyloxyphenyl)propionate (400 mg). According to the procedure described in the synthesis method of Compound of Example 001 (Preparation Method 4, Step d-1) with the modifications that the reaction was carried out for 16 hours, and the purification was performed by flash column chromatography (hexane:ethyl acetate=8:1), the above product was reacted with 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (360 mg), 2 M aqueous sodium carbonate (0.9 ml) and (Ph3P)4Pd (110 mg) and treated to obtain the title compound (Intermediate 66, 270 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06867320B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-e7064767dd5f43358df64e3811eae765 |
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| Source note | uspto-grants-2005_03 |
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