Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoroaniline | HCID 9584 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Reactant | 3-((alphaR)-alpha-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)-3-(tert-butyldimethylsilyloxy)benzyl)benzoyl chloride | HCID 11135038 | — |
| Product | HCID 21480431 | HCID 21480431 | — |
| Product | HCID 57238577 | HCID 57238577 | — |
Reaction Steps
2-Fluoro-N-propylaniline [NMR (DMSO-d6, 200 MHz): δ0.93 (t, J=7.4 Hz, 3H); 1.59 (m, 2H); 3.04 (q, 6.5 Hz, 2H); 5.33 (br m, 1H); 6.47-6.58 (m, 1H); 6.70 (t, J=8.1 Hz, 1H); 6.93-7.05 (m, 2H)] was prepared from 2-fluoroaniline and propionic anhydride, coupled with 3-((α-R)-α-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)-3-(tert-butyldimethylsilyloxy)benzyl)benzoyl chloride, deprotected and purified by the methods described in Example 10 to give (+)-3-((αR)-α-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)-3-hydroxybenzyl)-N-(2-fluorophenyl)-N-propylbenzamide as a white solid. NMR (DMSO-d6, 200 MHz): δ0.9-1.05 (m, 9H); 1.5 (m, 2H); 1.7 (m, 1H); 2.05 (m, 1H); 2.3 (m, 1H); 2.5 (m, 2H); 2.7 (m, 1H); 2.85 (m, 1H); 3.2 (m, 1H); 3.7 (m, 2H); 4.8 (br s, 1H); 5.1 (d, J=10 Hz, 1H); 5.2 (d, J=16 Hz, 1H); 5.8 (m, 1H); 6.5 (d, J=8 Hz, 1H); 6.6 (s, 1H); 6.65 (d, J=8 Hz, 1H); 7.0-7.4 (m, 9H); 9.3 (s, 1H). [α]D20 =+1.8° (abs ethanol., c=2.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05574159 |
|---|
| Source dataset | uspto-grants-1996_11 |
|---|
| ORD ID | ord-c23f0b611d6b4534af260a7487914b75 |
|---|
| Source note | uspto-grants-1996_11 |
|---|