HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzylamine → HCID 54682043, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | HCID 58739059 | HCID 58739059 | — |
| Product | HCID 54682043 | HCID 54682043 | — |
Reaction Steps
N-[(4-fluorophenyl)methyl]-1,6-dihydro-5-hydroxy-1-methyl-2-[4-(methylsulfonyl)-1-piperazinyl]-6-oxo-4-pyrimidinecarboxamide was synthesized from 5-hydroxy-2-(4-methanesulfonyl-piperazin-1-yl)-1-methyl-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid ethyl ester and 4-fluorobenzylamine as described in example to yield the title compound as a white solid 1H NMR (300 MHz, MeOD) δ: 8.88 (1H, t, J=5.9 Hz), 7.37 (2H, dd, J=8.6, 5.3 Hz), 7.05 (2H, t, J=8.8 Hz), 4.55 (2H, d, J=6.2 Hz), 3.55 (3H, s), 3.39–3.36 (4H, m), 3.26–3.23 (4H, m), 2.88 (3H, s). HRMS (M+H) calcd for C18H23FN5O5S: 440.14040. found: 440.1386.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135467B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-4f409ab7b72f4c36b2d75dcae5da160d |
| Source note | uspto-grants-2006_11 |