HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzamide → HCID 67250615, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzamide | HCID 2331 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | HCID 58327724 | HCID 58327724 | — |
| Product | HCID 67250615 | HCID 67250615 | — |
Reaction Steps
2-Acetamido-N-(3-((5-benzoyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-5-chlorophenyl)acetamide was synthesized using 2-acetamidoacetic acid and (4-((3-amino-5-chlorophenyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)(phenyl)methanone according to the procedure for the synthesis of N-3-((5-benzoyl-7H-pyrrolo[2,3-d]pyridine-4-yl)amino)phenyl)benzamide. A white solid was obtained. M.p.>300° C.; 400 MHz 1HNMR (DMSO-d6) δ 11.53 (s, 1H), 10.24 (s, 1H), 8.53 (s, 1H), 8.25-8.22 (m, 1H), 8.11-8.10 (m, 1H), 8.00 (d, J=2.0 Hz, 1H), 7.87 (s, 1H), 7.86-7.85 (m, 1H), 7.81-7.81 (m, 1H), 7.69-7.67 (m, 1H), 7.61-7.57 (m, 2H), 7.51-7.50 (m, 1H), 3.87 (d, J=6.0 Hz, 2H), 1.90 (s, 3H); LCMS [M+H] 463.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580803B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-4ab133081d46467aa658fff598a9ba17 |
| Source note | uspto-grants-2013_11 |