HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoromethanesulfonyl chloride → HCID 10049803, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoromethanesulfonyl chloride | HCID 79000 | — |
| Reactant | HCID 10042059 | HCID 10042059 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10049803 | HCID 10049803 | — |
Reaction Steps
By treatment of (3-aminomethyl-phenyl)-[4-(4-methyl-2-methylamino-thiazol-5-yl)-pyrimidin-2-yl]-amine with trifluoro-methanesulfonyl chloride. Yellow solid. Anal. RP-HPLC: tR=11.6 min (0-60% MeCN, purity ˜90%). 1H-NMR (CD3OD) δ: 2.53 (s, 3H, CH3), 2.97 (s, 3H, CH3), 4.39 (s, 2H, CH2), 6.94 (d, 1H, J=5.5 Hz, pyrimidinyl-H), 7.01 (d, 1H, J=7.5 Hz, Ph-H), 7.31 (d, 1H, J=8.0 Hz, Ph-H), 7.60 (d, 1H, J=7.5 Hz, Ph-H), 7.67 (s, 1H, Ph-H), 8.28 (d, 1H, J=5.5 Hz, pyrimidinyl-H). MS (ESI+) m/z 459.33 [M+H]+ (C17H17F3N6O2S requires 458.48).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897605B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-75f2aecd3877420296df2b9a924136cf |
| Source note | uspto-grants-2011_03 |