HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Bromomethyl)-2,4-difluorobenzene → HCID 10064279, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Bromomethyl)-2,4-difluorobenzene | HCID 90297 | — |
| Reactant | HCID 21892210 | HCID 21892210 | — |
| Reactant | HCID 86593739 | HCID 86593739 | — |
| Product | HCID 10064279 | HCID 10064279 | — |
Reaction Steps
2-Benzyloxy-6-(2,4-difluoro-benzyl)-1,6-dihydrodipyrrolo[3,2-d: 3′,4′-b]pyridin-3(2H)-one. The title compound was prepared by alkylation of 2-benzyloxy-1,6-dihydrodipyrrolo[3,2-d:3′,4′-b]pyridin-3(2H-one with 2,4-difluorobenzyl bromide in a manner similar to step (a) of example 1. 1H NMR (CD3OD) δ; 8.91 (s, 1H), 7.75 (d, 1H, J=3.0 Hz), 7.51–7.54 (m, 2H), 7.38–7.40 (m, 3H), 7.27–7.29 (m, 1H), 7.02–7.05 (m, 1H), 6.93–7.01 (m, 1H), 6.71 (d, 1H, J=3.0 Hz), 5.64 (s, 2H), 5.18 (s, 2H), 4.65 (s, 2H). LCMS (API-ES, M+H+): 406.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135482B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-5da99e67dfa34c9080f3adcea07bc90d |
| Source note | uspto-grants-2006_11 |