HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-2-methylindole → 7-(2-Methyl-1h-indol-5-ylamino)-thieno[3,2-b]pyridine-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-2-methylindole | HCID 2733992 | — |
| Reactant | 7-Chlorothieno[3,2-B]pyridine-2-carbonitrile | HCID 22278636 | — |
| Product | 7-(2-Methyl-1h-indol-5-ylamino)-thieno[3,2-b]pyridine-2-carbonitrile | HCID 22278676 | — |
Reaction Steps
The title compound was prepared from 2-methyl-1H-indol-5-ylamine and 7-chloro-thieno[3,2-b]pyridine-2-carbonitrile by a procedure analogous to Example 1C. MS: 305 (MH+), HPLC Rf: 4.86 min.; HPLC purity: 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06964961B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-ea492e3343604397b8c24af2ed92cbf4 |
| Source note | uspto-grants-2005_11 |