HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycinamide hydrochloride → HCID 58806151, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Reactant | 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy)-6-oxopyrimidin-1(6H)-yl]-N-[1-(aminocarbonyl)methyl]-4-methylbenzamide | HCID 21089008 | — |
| Product | HCID 58806151 | HCID 58806151 | — |
Reaction Steps
The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis of 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxopyrimidin-1(6H)-yl]-N-[1-(aminocarbonyl)methyl]-4-methylbenzamide by substituting (S)-3-hydroxypyrrolidine for glycineamide HCl. 1H NMR (CD3OD/400 MHz) δ8.31 (d, 1H, J=7.6 Hz), 7.62 (m, 2H), 7.52 (m, 2H), 7.01 (m, 2H), 5.59 (m, 2H), 4.42 .(m, 1H), 3.64 (m, 4H), 2.19 (s, 3H), 2.00 (m, 2H). ESHRMS m/z 476.1147 (M+H calculated for C23H21ClF2N3O4 requires 476.1183).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183287B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-f2559c47a3774fd08f9ce4c2ab627c3b |
| Source note | uspto-grants-2007_02 |