HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloropropionyl chloride → 1-(3-Chloropropanoyl)indoline-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloropropionyl chloride | HCID 69364 | — |
| Reactant | 2,3-dihydro-1H-indole-5-sulfonamide | HCID 8027252 | — |
| Reactant | 1-(Cyclohexanecarbonyl)indoline-5-sulfonamide | HCID 60698742 | — |
| Product | 1-(3-Chloropropanoyl)indoline-5-sulfonamide | HCID 86718887 | 98% |
Reaction Steps
Following a procedure analogous to that for the synthesis of Intermediate 55, indoline-5-sulfonamide (Intermediate 54A, 300 mg, 1.51 mmol) and 3-chloropropanoyl chloride (189 μL, 1.97 mmol) were converted to the title compound (430 mg, 98%). 1H NMR (DMSO-d6) δ 8.16 (d, J=8.1 Hz, 1H), 7.66-7.63 (m, 2H), 7.22 (s, 2H), 4.18 (t, J=8.6 Hz, 2H), 3.89-3.86 (m, 2H), 3.21 (t, J=8.5 Hz, 2H), 3.03 (t, J=6.4 Hz, 2H); MS (ESI+) m/z 289.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346795B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-7dd8c9ffe5be4bacaa2a95906a3ad15b |
| Source note | uspto-grants-2016_05 |