HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 44223336, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 44223627 | HCID 44223627 | — |
| Reactant | HCID 44223676 | HCID 44223676 | — |
| Product | HCID 44223336 | HCID 44223336 | 38% |
Reaction Steps
N-(3-chloro-2-(3-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide (38%) was prepared according to Example 25, substituting N-chlorosuccinimide for N-bromosuccinimide, DMF for CHCl3, and N-(2-(3-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide for 2,6-difluoro-N-(2-phenyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide. 1H NMR (400 MHz, DMSO-d6) δ 12.55 (s, 1H), 11.11 (s, 1H), 9.82 (s, 1H), 8.49-8.46 (m, 2H), 8.01-7.99 (m, 1H), 7.96-7.93 (m, 1H), 7.63-7.52 (m, 3H), 7.32-7.26 (m, 1H), 3.16-3.11 (m, 2H), 1.82-1.74 (m, 2H), 1.03-0.98 (m, 3H); m/z (APCI-pos) M+1=539.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338452B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-487f3250fc0141c7a8e588874bb903cd |
| Source note | uspto-grants-2012_12 |