HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178448767, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 21190634 | HCID 21190634 | — |
| Reactant | HCID 178509242 | HCID 178509242 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178448767 | HCID 178448767 | — |
Reaction Steps
Analogously to Example 32, 521 mg (2.00 mmol) of 3-amino-4-(3-chlorophenylamino)-1H-pyrazolo[3,4-d]pyrimidine (see Step 1.6) and 343 μl of acetic acid are dissolved in 50 ml of methanol and reacted with 691 mg (3.0 mmol) of 3-(2-tert-butyl-tetrazol-5-yl)-benzaldehyde to form 4-(3-chloro-phenylamino)-3-[{3-(2-tert-butyl-tetrazol-5-yl)-phenyl}-methyleneamino]-1H-pyrazolo[3,4-d]pyrimidine. Reduction of the above intermediate in 30 ml of DMEU with 16 ml (16 mmol) of DIBAL-H, analogous working-up and digestion in methanol yield 4(3-chloro-phenylamino)-3-[3(2-tert-butyl-tetrazol-5-yl)-benzylamino]1H-pyrazolo[3,4-d]pyrimidine; TLC: Rf=0.60 (CHCl3/methanol/H2O/acetic acid=85:13:1.5:0.5); HPLC: tRet(grad20-100)=10.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251911B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-00314e0ca70b45c5be9c67b4f796aa24 |
| Source note | uspto-grants-2001_06 |