HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 44223177, compound → HCID 67155679, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 44223177 | HCID 44223177 | — |
| Reactant | HCID 67156141 | HCID 67156141 | — |
| Product | HCID 67155679 | HCID 67155679 | — |
Reaction Steps
2,6-Difluoro-N-(2-(3-hydroxypropyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide was prepared according to the general procedure of Example 95 substituting 2,6-difluoro-N-(2-(3-hydroxyprop-1-ynyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide for N-(2-(3-(dimethylamino)prop-1-ynyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide. 1H NMR (400 MHz, CD3OD) δ 8.28-8.21 (m, 2H), 7.67-7.61 (m, 1H), 7.15-7.09 (m, 1H), 6.24 (s, 1H), 3.66-3.62 (m, 2H), 3.13-3.09 (m, 2H), 2.90-2.85 (m, 2H), 2.01-1.84 (m, 2H), 1.08-1.03 (m, 3H); m/z (APCI-pos) M+1=453.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338452B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-f11188e802df4dbb9e6b115cb6165db4 |
| Source note | uspto-grants-2012_12 |