HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 54088438, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | (1-Benzyl-1H-indazol-5-yl)-(6-iodoquinazolin-4-yl)-amine | HCID 21952131 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54088438 | HCID 54088438 | 17.6% |
Reaction Steps
(1-Benzyl-1H-indazol-5-yl)-(6-iodoquinazolin-4-yl)-amine (0.48 g) in DMF under CO was treated with sodium formate (0.1 g) and catalytic quantities of triphenyl phosphine and bistriphenylphosphine palladium (II) chloride at 110° C. The mixture was cooled, added to 5% sodium hydroxide and extracted with ethyl acetate. The aqueous phase was treated with 2N HCl and the precipitated solid filtered and dried to give the title compound (0.07 g); δH [2H6]DMSO 13.35(1H,bs), 10.40(1H,s), 9.30(1H,s), 8.60(1H,s), 8.30(1H,d), 8.17(2H,d), 7.84(1H,d), 7.72(1H,s), 7.30(5H,m,), 5.70(2H,s); m/z (M+1)+396.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06391874B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-17ca6e946a0c4fda878297b0ee1b11ce |
| Source note | uspto-grants-2002_05 |