HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 57773637, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Iodobenzoyl chloride | HCID 74373 | — |
| Reactant | HCID 68630202 | HCID 68630202 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57773637 | HCID 57773637 | — |
Reaction Steps
To a round bottom flask containing 1-amino-2,3-dihydro-1H-indene-5-sulfonamide hydrochloride salt (93 mg, 0.38 mmol) suspended in dichloromethane (3 mL) was added triethylamine (61 μL) followed by 4-iodobenzoylchloride (100 mg, 0.38 mmol) and the reaction was stirred overnight at room temperature. The reaction was diluted with dischloromethane (25 mL) and washed with 10% aqueous hydrochloric acid (10 mL), water (10 mL), brine (10 mL), dried over sodium sulfate and concentrated to afford the crude material as an off-white solid. Recrystallization from ethanol/water afforded MIP-1146 (19 mg, 21%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.96 (m, 2H), 7.85-7.35 (m, 8H), 5.60 (m, 1H), 3.15-2.75 (m, 2H), 2.15-1.90 (m, 2H); (M+H)+ (443).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877970B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-7ab8d123285749b492c39b32ae227aef |
| Source note | uspto-grants-2014_11 |