HuagongsheHuagongshe Chemistry Print Report · For research reference only
826-62-0 → HCID 67532003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 826-62-0 | HCID 13223 | — |
| Reactant | HCID 67531620 | HCID 67531620 | — |
| Reactant | HCID 67531839 | HCID 67531839 | — |
| Product | HCID 67532003 | HCID 67532003 | 94% |
Reaction Steps
Following the same procedure to synthesize 2-(2-amino-1H-benzo[d]imidazol-6-ylcarbamoyl)benzoic acid hydrochloride (8), tert-butyl 6-amino-2-(bis(tert-butoxycarbonyl)amino)-1H-benzo[d]imidazole-1-carboxylate (0.114 g, 0.254 mmol) was reacted with Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride (0.042 g, 0.254 mmol) to make the title product (0.084 g, 94% yield) as a white solid. 1H NMR (300 MHz, CD3OD) δ 7.35 (d, 1H), δ 7.13 (s, 1H), δ 6.99 (d, 1H), δ 6.23 (s, 2H), δ 3.51 (s, 2H), δ 3.37 (s, 2H), δ 1.68 (dd, 2H) ppm; 13C NMR (75 MHz, CD3OD) δ 178.1, 151.7, 134.8, 134.6, 130.6, 129.8, 129.6, 128.1, 122.8, 111.5, 110.7, 52.0, 46.8, 45.9, 45.5, 45.4 ppm; HRMS (ESI) Calcd for C16H16N4O3 (M+) 312.1222. Found 312.1226.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221765B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-3ee5dcb767be408491d55f483b8663f2 |
| Source note | uspto-grants-2015_12 |