HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479815Generated: October 26, 2026
Diethyl Pyrocarbonate → 2-[(4-chlorophenyl)sulfonyl-ethyl-amino]-N-[[2-[4-(trifluoromethoxy)phenyl]-4-pyridyl]methyl]prop-2-enamide
https://huagongshe.com/reaction/1479815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Pyrocarbonate | HCID 3051 | — |
| Reactant | [2-[4-(Trifluoromethoxy)phenyl]-4-pyridyl]methanamine | HCID 68759664 | — |
| Reactant | 2-[(4-Chlorophenyl)sulfonyl-ethyl-amino]prop-2-enoic acid | HCID 131736586 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(4-chlorophenyl)sulfonyl-ethyl-amino]-N-[[2-[4-(trifluoromethoxy)phenyl]-4-pyridyl]methyl]prop-2-enamide | HCID 78319912 | 18.5% |
Reaction Steps
Acid 4D (221.45 mg, 1 mmol) was dissolved in 10 ml of THF and at rt DEPC (1.1 equiv, 0.15 ml) and [2-[4-(trifluoromethoxy)phenyl]-4-pyridyl]methanamine 21B (1.1 equiv., 295 mg) were added to the solution. The mixture was stirred at rt overnight then evaporated. The residue was dissolved in EtOAc (30 ml) and washed with water (1×20 ml) and brine. The organic phase was dried over sodium sulfate and concentrated under vacuum. The purification of the crude by chromatographic column (3:7 EtOAc:petroleum ether) afforded 100 mg of a white solid. Yield=18.5% 1HNMR (DMSO, 400 MHz) δ 1.08 (3H, t), 3.40 (2H, q), 4.42 (2H, d), 5.20 (1H, s), 6.08 (1H, s), 7.23 (1H, d), 7.45 (2H, d), 7.72 (4H, dd), 7.85 (1H, s), 8.20 (2H, d), 8.60 (1H, d), 8.74 (1H, bt) [M+1] 540.1 (C24H21ClF3N3O4S requires 539.95).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09409864B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-d2f0263cf6854cb5a0dcacc249fb0619 |
|---|
| Source note | uspto-grants-2016_08 |
|---|