HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propionyl chloride → 2-methyl-N-(3-{1-[(3S)-3-phenyl-3-(propionylamino)propyl]-4-piperidinyl}phenyl)propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | N-(3-{1-[(3S)-3-(acetylamino)-3-phenylpropyl]-4-piperidinyl)phenyl)-2-methylpropanamide | HCID 69523292 | — |
| Reactant | N-(3-(1-[(3S)-3-amino-3-phenylpropyl]-4-piperidinyl)phenyl)-2-methylpropanamide | HCID 69523474 | — |
| Product | 2-methyl-N-(3-{1-[(3S)-3-phenyl-3-(propionylamino)propyl]-4-piperidinyl}phenyl)propanamide | HCID 20722976 | 97% |
Reaction Steps
According to the procedure used for the synthesis of N-(3-{1-[(3S)-3-(acetylamino)-3-phenylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide, N-(3-{1-[(3S)-3-amino-3-phenylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide (11.0 mg, 0.0280 mmol) and propionyl chloride (3.80 mg, 0.0420 mmol) provided 2-methyl-N-(3-{1-[(3S)-3-phenyl-3-(propionylamino)propyl]-4-piperidinyl}phenyl)propanamide (12 mg, 97% yield). 1H NMR (400 MHz, CDCl3) δ 8.05 (s, 1H), 7.59 (s, 1H), 7.40–7.20 (m, 7H), 6.96 (s, 1H), 5.19–5.12 (m, 1H), 3.18 (d, 1H, J=12.0 Hz), 2.99 (d, 1H, J=10.4 Hz), 2.93–2.86 (m, 1H), 2.61–2.40 (m, 3H), 2.38–2.23 (m, 3H), 2.19–1.75 (m, 8H), 1.25 (d, 6H, J=6.9 Hz), 1.22–1.08 (m, 3H); ESMS m/e: 436.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067534B1 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-64f926a398ef46f8a2f8cbe0b0f63906 |
| Source note | uspto-grants-2006_06 |