HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Hydroxy-2-methyl-1h-indole-3-carbonitrile → HCID 10165314, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Hydroxy-2-methyl-1h-indole-3-carbonitrile | HCID 22250077 | — |
| Reactant | HCID 22250086 | HCID 22250086 | — |
| Product | HCID 10165314 | HCID 10165314 | 41% |
Reaction Steps
The title compound (61 mg, 41%) was prepared from [2-(7-Chloro-thieno[3,2-b]pyridin-2-yl)-4-methyl-thiazol-5-yl]-(4-methyl-piperazin-1-yl)-methanone and 5-Hydroxy-2-methyl-1 H-indole-3-carbonitrile by a procedure analogous to Example 16 using and in a 41% yield. C27H25N6O2S2: APCI m/z 529.4 (pos.); 1H NMR (CD3OD): δ 8.72 (d, 1H, J=6.6 Hz), 8.17 (s, 1H), 7.60 (d, 1H, J=8.7 Hz), 7.58 (s, 1H), 7.23 (d, 1H, J=8.7 Hz), 7.07 (d, 1H, J=6.6 Hz), 3.65–3.15 (bm, 8H), 2.96 (s, 3H), 2.63 (s, 3H), 2.52 (s, 3H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06995171B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-2cbfdd10cb9642f4bea03e9386e3f881 |
| Source note | uspto-grants-2006_02 |