HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363083Generated: October 29, 2026
Benzenesulfonyl chloride → (S)-N-(6-Cyano-1,2,3,4-tetrahydro-quinolin-3-yl)-benzenesulfonamide
https://huagongshe.com/reaction/1363083
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (S)-3-Amino-1,2,3,4-tetrahydroquinoline-6-carbonitrile | HCID 66757521 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-N-(6-Cyano-1,2,3,4-tetrahydro-quinolin-3-yl)-benzenesulfonamide | HCID 66757946 | 90.4% |
Reaction Steps
To a suspension of 1F (103.9 mg, 0.6 mmol) in CH3CN (3 mL) at RT under argon was added DIPEA (0.11 mL, 0.66 mmol), followed by dropwise addition of benzene sulfonylchloride (0.08 mL, 0.63 mmol). The reaction mixture was stirred at RT for 1.5 h, then concentrated under reduced pressure. The residue was taken into EtOAc, washed with water, brine, dried (Na2SO4), and concentrated. The resulting residue was chromatographed (silica gel) eluting with EtOAc (30-50%) in hexane to give the title compound (170 mg, 90%). HPLC: 99% at 5.2 min (retention time) (Conditions: Zorbax SB C18 (4.6×75 mm); Eluted with 0% to 100% B, 8 min gradient. (A=90% H2O−10% MeOH−0.1% H3PO4 and B=10% H2O−90% MeOH−0.1% H3PO4); Flow rate at 2.5 mL/min. UV detection at 220 nm). MS (ES): m/z 314 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07884113B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-2171d778a608484f836b6ae9235492e0 |
|---|
| Source note | uspto-grants-2011_02 |
|---|