HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-((3-Chloropropyl)sulfonyl)-4-methylpiperazine → HCID 178481109, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-((3-Chloropropyl)sulfonyl)-4-methylpiperazine | HCID 10243385 | — |
| Reactant | N-(7-hydroxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)pyridine-3-carboxamide | HCID 178522515 | — |
| Product | HCID 178481109 | HCID 178481109 | — |
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 1-[(3-chloropropyl)sulfonyl]-4-methylpiperazine (Intermediate D). High vacuum drying at 60° C. gave the title compound (72 mg, 57%): HPLC MS RT=1.22 min, MH+=512.2; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 2.26-2.31 (2H, m), 2.82 (3H, s), 3.11-3.21 (4H, m), 3.45-3.50 (4H, m), 3.83-3.87 (2H, m), 4.27-4.34 (2H, m), 4.42 (2H, t), 4.58-4.65 (2H, m), 7.60 (1H, t), 7.73 (1H, d), 7.85 (1H, d), 7.94 (1H, dd), 8.86 (1H, d), 9.00 (1H, dd), 9.48 (1H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859572B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-7c5c1fb74c6045b59bc8fb62e844cf25 |
| Source note | uspto-grants-2014_10 |