HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 59239561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Ethyl-3-(4-(4-morpholino-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl) phenyl)urea | HCID 46913071 | — |
| Product | HCID 59239561 | HCID 59239561 | 4.4% |
Reaction Steps
To a solution of 1-ethyl-3-(4-(4-morpholino-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2-yl)phenyl)urea (bf) (115 mg, 0.300 mmol) in N,N-Dimethylformamide (2.00 mL) and N,N-Diisopropylethylamine (0.104 mL, 0.600 mmol) was added 6-chloror-1-methylpyridin-2(1H)-one (129 mg, 0.90 mmol) at room temperature. The reaction was kept at 140° C. overnight, followed by RPHPLC purification. The desired product pv (6.4 mg, 4.4% yield) was obtained as white powder: 1H NMR (400 MHz, DMSO) δ 8.64 (s, 1H), 8.19 (d, J=8.8 Hz, 2H), 7.48 (d, J=8.8 Hz, 2H), 7.38 (m, 1H), 6.19-6.10 (m, 2H), 6.01 (d, J=6.6, 1H), 4.15 (s, 2H), 3.80-3.71 (m, 4H), 3.53 (m, 4H), 3.48 (s, 3H), 3.24-3.06 (m, 4H), 2.86 (s, 2H), 1.06 (t, J=7.2 Hz, 3H); LC-MS m/z=490 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163763B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-c1058736d2b84043bbe688c16435d086 |
| Source note | uspto-grants-2012_04 |