HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycinamide hydrochloride → HCID 58806168, 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 58806168 | HCID 58806168 | — |
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)-(+)-2-amino-1-propanol for glycineamide HCl. 1H NMR (CD3OD/400 MHz) δ8.32 (s, 1H), 7.92 (m, 1H), 7.77 (s, 1H), 7.61 (q, 1H, J=8.4 Hz), 7.52 (d, 1H, J=8.0 Hz), 7.02 (m, 2H), 5.60 (m, 2H), 4.16 (m, 1H), 3.58 (m, 2H), 2.20 (s, 3H), 1.22 (d, 3H, J=6.0 Hz). ESHRMS m/z 464.1198 (M+H calculated for C22H21ClF2N3O4 requires 464.1183).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183287B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-ff9b7476bfa34a08865e627ec11c0ee2 |
| Source note | uspto-grants-2007_02 |