HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-chloro-N,N-dimethylpropane-1-sulfonamide → HCID 178486161, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-chloro-N,N-dimethylpropane-1-sulfonamide | HCID 10035328 | — |
| Reactant | N-(7-hydroxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)pyridine-3-carboxamide | HCID 178522515 | — |
| Product | HCID 178486161 | HCID 178486161 | — |
Reaction Steps
The procedure used for the preparation of Example 1 was used to prepare the title compound from N-(7-hydroxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)nicotinamide (Intermediate C) and 3-chloro-N,N-dimethylpropane-1-sulfonamide (Intermediate F). High vacuum drying at 60° C. gave the title compound (44 mg, 39%): HPLC MS RT=0.68 min, MH+=457.3; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 2.27 (2H, bs), 2.84 (6H, s), 3.36-3.37 (2H, m), 4.31 (2H, bs), 4.43 (2H, bs), 4.62 (2H, bs), 7.59-7.61 (1H, m), 7.71 (1H, bs), 7.83-7.86 (1H, m), 7.97-7.98 (1H, m), 8.89 (1H, bs), 9.00 (1H, m), 9.47 (1H, bs).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859572B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-b1e3982288a7426eb17e76c56f67ad5c |
| Source note | uspto-grants-2014_10 |