HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[3-(7-Fluoro-quinolin-6-ylmethyl)-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl]-ethanone → HCID 58190581, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[3-(7-Fluoro-quinolin-6-ylmethyl)-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl]-ethanone | HCID 58190578 | — |
| Reactant | HCID 69813455 | HCID 69813455 | — |
| Product | HCID 58190581 | HCID 58190581 | 57.4% |
Reaction Steps
The title compound (7.0 mg, 50%) was synthesized from 1-[3-(7-fluoro-quinolin-6-ylmethyl)-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl]-ethanone (15.4) (10.0 mg, 0.03 mmol) and (R)—O-pyrrolidin-3-yl-hydroxylamine hydrochloride (10.8 mg, 0.06 mmol) using the same procedure as described in the synthesis of example 15. 1H-NMR (400 MHz, DMSO-d6) δ ppm 9.31 (s, 1H), 8.93 (d, 1H), 8.40 (d, 1H), 8.16 (d, 1H), 7.83 (d, 1H), 7.54 (dd, 1H), 6.24 (s, 2H), 4.95 (m, 1H), 3.01-2.87 (m, 3H), 2.74-2.67 (m, 1H), 2.27 (s, 3H), 2.15-1.90 (m, 2H). LCMS (method A): [MH]+=407, tR=3.98 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410264B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-b885d0f4ac1f494485657ac2e197e920 |
| Source note | uspto-grants-2013_04 |