HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-(-)-2-Amino-1-propanol → HCID 21088983, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-(-)-2-Amino-1-propanol | HCID 80308 | — |
| Reactant | HCID 58806160 | HCID 58806160 | — |
| Product | HCID 21088983 | HCID 21088983 | — |
Reaction Steps
The title compound was prepared using a procedure similar to that used in Step 5 of the synthesis of 3-[4-[(2,4-difluorobenzyl)oxy]-5-ethyl-6-oxopyrimidin-1(6H)-yl]-N-[(1R)-2-hydroxy-1-methylethyl]-4-methylbenzamide by substituting ethanolamine for (R)-(−)-2-amino-1-propanol. 1H NMR (CD3OD/400 MHz) δ8.19 (s, 1H), 7.90 (m, 1H), 7.73 (s, 1H), 7.57 (q, 1H, J=8.4 Hz), 7.51 (d, 1H, J=8.0 Hz), 7.00 (m, 2H), 5.51 (q, 2H, J=12.4 Hz), 3.69 (t, 2H, J=6.0 Hz), 3.48 (t, 2H, J=5.6 Hz), 2.51 (q, 2H, J=7.6 Hz), 2.17 (s, 3H), 1.05 (t, 3H, J=7.6 Hz). ESHRMS m/z 444.1704 (M+H calculated for C23H24F2N3O4 requires 444.1729).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183287B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-010fbe0b6a8a49a7b8596feba42197dc |
| Source note | uspto-grants-2007_02 |