HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173161Generated: October 30, 2026
Potassium Phosphate, Tribasic → HCID 24746279, compound
https://huagongshe.com/reaction/1173161
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | Ethyl 6-bromo-1-benzothiophene-2-carboxylate | HCID 13567982 | — |
| Reactant | tert-Butyl 2,8-diazaspiro[4.5]decane-2-carboxylate | HCID 34178604 | — |
| Reactant | N-(3-Amino[1,1'-biphenyl]-4-yl)-carbamic Acid tert-Butyl Ester | HCID 57717454 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | HCID 24746279 | HCID 24746279 | — |
Reaction Steps
A mixture of ethyl 6-bromo-1-benzothiophene-2-carboxylate (250 mg, 0.88 mmol), tert-butyl 2,8-diazaspiro[4.5]decane-2-carboxylate (200 mg, 0.83 mmol), and K3PO4 (1.00 g, 4.72 mmol) in 2 mL of DMAc was deoxygenated by the freeze-pump-thaw method. The mixture was treated with Pd[P(tert-Bu)3]2 (130 mg, 0.250 mmol) and stirred at 90° C. overnight. The reaction mixture was partitioned between EtOAc and sat'd NaHCO3, the organic layer dried (Na2SO4), filtered and concentrated. The residue was dissolved in 1 mL of MeOH, 1 mL of THF and 1 mL of H2O, treated with LiOH monohydrate (100 mg, 2.40 mmol) and stirred for 12 h. The mixture was poured into EtOAc and washed with 2 N HCl, water, dried (Na2SO4), filtered and concentrated. The oily residue was dissolved in 2 mL of DM, treated with intermediate C (200 mg, 0.980 mmol), BOP (300 mg, 0.679 mmol), i-Pr2NEt (0.250 mL, 1.41 mmol) and stirred for 1 day at ambient temperature followed by 5 days at 60° C. The mixture was partitioned between EtOAc and sat'd NaHCO3, the organic layer was dried (Na2SO4) and concentrated. Chromatography on SiO2 (0 to 100% EtOAc/CH2Cl2) gave pure intermediate. The oil was stirred in 2 mL of 1:1 TFA/CH2Cl2 for 1 h and concentrated. The oil was dissolved in EtOAc, washed with sat'd NaHCO3, dried (Na2SO4) and concentrated, providing the title compound: MS (ESI+): cal'd [M+H]+ 483.2, obs'd 483.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834026B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-ad2bfb6e1ced4c488b88f7705658b6d8 |
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| Source note | uspto-grants-2010_11 |
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