HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → N-[(S)-2-(3,4-Dichlorophenyl)-4-(phenylamino)butyl]-N-methyl-2-methoxy-3-cyano-1-naphthamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | N-[(S)-2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methyl-2-methoxy-3-cyano-1-naphthamide | HCID 11091697 | — |
| Product | N-[(S)-2-(3,4-Dichlorophenyl)-4-(phenylamino)butyl]-N-methyl-2-methoxy-3-cyano-1-naphthamide | HCID 69859768 | — |
Reaction Steps
N-[(S)-2-(3,4-Dichlorophenyl)-4-oxobutyl]-N-methyl-2-methoxy-3-cyano-1-naphthamide was reacted with aniline under standard reductive amination conditions to give the title compound which was converted to the citrate salt. 1H NMR(300 MHz, DMSO-d6) δ8.64-8.61 (m), 8.07-7.98 (m), 7.79-7.55 (m), 7.51-7.47 (m), 7.37-7.32 (t), 7.08-7.00 (m), 6.53-6.49 (m), 6.31-6.28 (d), 4.60-4.50 (t), 4.07-3.96 (m), 3.92 (s), 3.90-3.78 (m), 3.86 (s), 3.45-3.11 (m), 3.00-2.88 (m), 2.79 (s), 2.73 (s), 2.68 (s), 2.56-2.44 (m), 2.03-1.88 (m); MS APCI, m/z=532 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476077B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-4ea2a463a8d641c6acb2edc207205ab4 |
| Source note | uspto-grants-2002_11 |