HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 71209178, compound → HCID 86675743, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 71209178 | HCID 71209178 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86675743 | HCID 86675743 | 73.3% |
Reaction Steps
To a solution of (1-(3,4-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)methanol (5.0 g, 8.45 mmol) in DCM (85 mL) at 0° C. was added PCC (3.64 g, 16.90 mmol) and the mixture was stirred at RT for 4 h. The mixture was adsorbed on silica gel and purified by column chromatography to provide 1-(3,4-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde (3.0 g, 6.19 mmol, 73.2% yield) as an off-white solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 2.91 (s, 3 H), 5.45 (s, 2 H), 6.56 (d, J=3.71 Hz, 1 H), 6.91-7.19 (m, 3 H), 7.22 (d, J=3.51 Hz, 1 H), m10.40 (s, 1H); LCMS (m/z) ES+=413 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609653B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-cafd4d300be54a16ab40c9e4ad91a371 |
| Source note | uspto-grants-2013_12 |