HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Phenylmethyl)-1H-indazol-5-amine → (1-Benzyl-1H-indazol-5-yl)-(6-(5-methyl-1,3,4-oxadiazol-2-yl)-pyrido[3,4-d]pyrimidin-4-yl)-amine Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Phenylmethyl)-1H-indazol-5-amine | HCID 212069 | — |
| Reactant | HCID 22011950 | HCID 22011950 | — |
| Product | (1-Benzyl-1H-indazol-5-yl)-(6-(5-methyl-1,3,4-oxadiazol-2-yl)-pyrido[3,4-d]pyrimidin-4-yl)-amine Hydrochloride | HCID 22727467 | — |
Reaction Steps
4-Chloro-6-(5-methyl-1,3,4-oxadiazol-2-yl) pyrido[3,4-d]pyrimidine (0.02 g) was reacted with 1-benzylindazol-5-ylamine according to Procedure A to give the title compound as a yellow solid; δH [2H6]DMSO 11.50(1H,s), 9.55(1H,s), 9.43(1H,s), 8.95(1H,s), 8.34(2H,m),7.91(1H,d) 7.83(1H,dd),7.40(5H,m), 5.80(2H,s), 2.75 (3H,s); m/z (M+1+) 435.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174889B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-273541907f1441e090bcd238b5aa4147 |
| Source note | uspto-grants-2001_01 |