HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 59993290, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cyano-borohydride | HCID 498716 | — |
| Reactant | HCID 59993356 | HCID 59993356 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59993290 | HCID 59993290 | — |
Reaction Steps
To a mixture of 2-{1-[1-(4-methoxy-benzenesulfonyl)-piperidin-4-ylamino]-ethyl}-3-methyl-3H-quinazolin-4-one (183 mg, 0.4 mmol), formaldehyde (39 μL, 0.48 mmol, 37% wt. solution in water) and DMF (1 mL) was added MP-Cyanoborohydride (300 mg, 2-3 mmol/g) and the reaction was stirred overnight at room temperature. The reaction mixture was then filtered and purified by HPLC to yield the product. HPLC ret. time 2.41 min, 10-99% CH3CN, 5 min run; 1H NMR (400 MHz, CDCl3) δ 8.28 (d, J=8.0 Hz, 1H), 7.93 (t, J=7.2 Hz, 1H), 7.68 (m, 4H), 7.03 (d, J=8.6 Hz, 2H), 4.93 (m, 1H), 3.98 (s, 1H), 3.89 (s, 3H), 3.69 (s, 3H), 3.10 (s, 3H), 2.58 (m, 2H), 2.21 (m, 2H), 1.78 (d, J=6.6 Hz, 3H), 1.31 (m, 4H); ESI-MS m/z 471.3 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642609B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-395625dd0afe4030aaa0fe575ed061f3 |
| Source note | uspto-grants-2014_02 |