Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 68717065 | HCID 68717065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68715097 | HCID 68715097 | 83% |
Reaction Steps
Ethyl 4-{[4-(tert-butoxycarbonyl)piperazin-1-yl]methyl}-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-carboxylate (330 mg, 0.6 mmol, Intermediate 56) was dissolved in THF (10 mL) before lithium hydroxide (17 mg, 0.7 mmol) was added followed by 4 mL water. The reaction mixture was heated to 70° C. for 24 h before the reaction was completed. The reaction mixture was evaporated. This gave 3 g of a white solid which was washed with several portions of hot DCM and then hot THF. The combined wash phases were evaporated. This gave 270 mg of a slightly brown solid. Yield 83%. MS (ESI+) for C26H30N3O7SLi m/z 530 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812017B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-b5d8c0c46af84005b3e8f698b853e1f6 |
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| Source note | uspto-grants-2010_10 |
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