HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507705Generated: October 29, 2026
Diisopropylethylamine → HCID 69331416, compound
https://huagongshe.com/reaction/507705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 4-amino-N-(tert-butoxycarbonyl)-L-phenylalaninate | HCID 10638537 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | HCID 69331416 | HCID 69331416 | 77.4% |
Reaction Steps
Ethyl (S)-3-(4-aminophenyl)-2-[N-(t-butyloxycarbonyl)amino]propanoate (600 mg, 1.95 mmol), Intermediate 21 (350 mg, 2.13 mmol) and DIPEA (276 mg, 372 μl, 2.13 mmol) in 2-ethoxyethanol (0.5 ml) were stirred at 130° under N2 for several hours. The reaction was partitioned between EtOAc (70 ml) and saturated aqueous NaHCO3 (30 ml). The phases were separated and the aqueous layer re-extracted with EtOAc (3×30 ml). The combined organic extracts were washed with brine (10 ml), dried (MgSO4) and evaporated in vacuo to afford a dark oil. Chromatography (SiO2; 3% MeOH/DCM) gave the title compound as a dull orange foam (360 mg, 42%). δH (CDCl3) 9.19 (1H, s), 8.67 (1H, d, J 5.9 Hz), 8.24 (1H, d, J 5.8 Hz), 7.66 (1H, d, J 5.9 Hz), 7.65 (2H, d, J 8.5 Hz), 7.21 (1H, d, J 5.8 Hz), 7.16 (2H, d, J 8.5 Hz), 7.15 (1H, obscured s), 5.05-4.97 (1H, m), 4.60-4.51 (1H, m), 4.19 (2H, q, J 7.1 Hz), 3.17-3.04 (2H, m), 1.44 (9H, s), 1.27 (3H, t, J 7.1 Hz); m/z (ES+, 70V) 459 (MNa+), 437 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07786177B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-3699b0d1afbd4500b912374aafbe227d |
|---|
| Source note | uspto-grants-2010_08 |
|---|