HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902956Generated: October 30, 2026
Triethylamine → n-[1-Benzyloxycarbonyl-2-(1h-indol-3-yl)-ethyl]-3-{[benzyloxy-(4-phenyl-butyl)-phosphinoyl]-amino}-succinamic acid benzyl ester
https://huagongshe.com/reaction/902956
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bistrimethylsilylacetamid | HCID 11708267 | — |
| Reactant | Acetonitrile tetrachloromethane | HCID 18669661 | — |
| Reactant | H-Asp(OBn)-Trp(OBn) | HCID 131725939 | — |
| Reactant | HCID 178527035 | HCID 178527035 | — |
| Product | n-[1-Benzyloxycarbonyl-2-(1h-indol-3-yl)-ethyl]-3-{[benzyloxy-(4-phenyl-butyl)-phosphinoyl]-amino}-succinamic acid benzyl ester | HCID 69212717 | 44% |
Reaction Steps
To a stirred solution of the phosphinate of Example 81 (144 mg, 0.50 mmol) in dry degassed acetonitrile (1.5 mL), was added bis-(trimethylsilyl)acetamide (73 μL, 0.30 mmol) followed immediately by the addition of a solution of H-Asp(OBn)-Trp(OBn), [Example 83 (322 mg, 0.60 mmol)] and Et3N (209 μL, 1.5 mmol) in CCl4/CH3CN (3:1, 2 mL). The reaction mixture was stirred at room temperature for 14 h and then concentrated in vacuum. Purification by flash chromatography using a gradient of EtOAc in hexane (50% to 100%) provided the title compound (0.175 g, 44%) as a white residue: Rf l(100% EtOAc)=0.5; 1H NMR (CDCl3) δ 8.5 (d, 1H), 7.6 (d, 1H), 7.5-6.9 (m, 25), 5.2-4.9 (m, 6H), 4.83 (dd, 1H), 4.63 (dd, 1H), 4.22 (m, 1H), 3.91(d, 1H), 3.36 (dt, 1H), 3.28 (dt,1H), 3.01 (dd, 1H), 2.65 (dt, 1H), 2.50 (m, 2H), 1.71-1.25 (m, 6H); 31P NMR (CDCl3) δ 35.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365091B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-b9c4e48f4bfa4eae8ee5aa82681774b7 |
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| Source note | uspto-grants-2008_04 |
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