HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glutaric anhydride → HCID 67532267, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glutaric anhydride | HCID 7940 | — |
| Reactant | HCID 67531620 | HCID 67531620 | — |
| Reactant | HCID 178479113 | HCID 178479113 | — |
| Product | HCID 67532267 | HCID 67532267 | 93% |
Reaction Steps
Following the same procedure to synthesize 1-(2-amino-1H-benzo[d]imidazol-6-yl)-1H-pyrrole-2,5-dione hydrochloride, tert-butyl 6-amino-2-(bis(tert-butoxycarbonyl)amino)-1H-benzo[d]imidazole-1-carboxylate (0.113 g, 0.252 mmol) was reacted with glutaric anhydride (0.029 g, 0.252 mmol) to give the title compound (0.066 g, 93% yield) as a white solid. 1H NMR (300 MHz, CD3OD) δ 7.85 (s, 1H), δ 7.28 (s, 2H), δ 2.42 (m, 4H), δ 1.97 (m, 2H) ppm; 13C NMR (75 MHz, CD3OD) δ 174.1, 172.6, 135.2, 129.8, 125.9, 103.6, 35.6, 32.9, 20.9 ppm; HRMS (ESI) Calcd for C12H12N4O2 (M+) 244.0960. Found 244.0969.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221765B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-887639567cb14a449c56343b539c93ea |
| Source note | uspto-grants-2015_12 |