HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 57504478, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | HCID 57504584 | HCID 57504584 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57504478 | HCID 57504478 | — |
Reaction Steps
Trimethylsilyldiazomethane (2 M in diethyl ether) was added slowly to a stirred solution of N-[1-(2-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]glycine (Step 1) (0.80 g, 2.63 mmol) in DCM (4 mL) and MeOH (1 mL) until a yellow colour persisted. A few drops of acetic acid was added after 1 minute followed by the addition of DCM and water. The two phases were separated and the organic phase was concentrated in vacuo to give the title compound (795 mg), 1H NMR (300 MHz, CD3OD) δ 8.32 (s, 1H), 8.24 (s, 1H), 7.66 (m, 1H), 7.54 (m, 3H), 4.39 (s, 2H), 3.77 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143263B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-ae8d98b7b372499f9a52f21883356fbf |
| Source note | uspto-grants-2012_03 |