HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648120Generated: November 2, 2026
HCID 70046131, compound → HCID 86748805, compound
https://huagongshe.com/reaction/1648120
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 70046131 | HCID 70046131 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86748805 | HCID 86748805 | 71.2% |
Reaction Steps
To a solution of 195 mg of N-(3-(4-hydroxyphenyl)propionyl-valinyl-alaninyl)-4-amino-5-benzyloxy-2-oxotetrahydrofuran in 5 mL of methanol was added ~100 mg of Pd(OH)2 on carbon. After the mixture had been stirred vigorously under hydrogen for 3 hours, the mixture was filtered through a 0.22 μm nylon membrane filter and concentrated. The residue was purified by MPLC on silica-gel (22×300 mm column, eluted with a gradient of dichloromethane to 8% formic acid and 32% methanol in dichloromethane) to afford 115 mg of the title compound as a colorless solid: 1H NMR (400 MHz, CD3OD (1:1 mixture of diastereomeric hemiacetals in this solvent)) δ7.01 (d, 2H, J=8.39 Hz, Ar--H), 6.67 (d, 2H, J=8.53 Hz, Ar--H), 4.58 (d, 0.5H, J=3.92 Hz, CH(OH)(OCD3)), 4.56 (d, 0.5H, J=4.06 Hz, CH(OH)(OCD 3)), 4.34 (m, 1H, CHN), 4.24 (m, 1H, CHN), 4.09 (d, 1H, J=7.10 Hz, CHN), 2.81 (t, 2H, J=7.56 Hz, CH2CON), 2.7-2.4 (m, 4H, CH2Ar, CH2CO2), 2.00 (m, 1H, CH(CH3)2), 1.32 (d, 3H, J=5.81Hz, CHCH3), 0.89 (d, 3H, J=6.82 Hz, CH(CH3)2), 0.85 (d, 3H, J=6.87 Hz, CH(CH3)2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05434248 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-21b6a0edc6074e8aae6ff230d4ef1e8a |
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| Source note | uspto-grants-1995_07 |
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