HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-amino-2H-1,3-benzodiazol-2-one → HCID 67391805, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-amino-2H-1,3-benzodiazol-2-one | HCID 15250547 | — |
| Reactant | 5-Nitro-2H-benzimidazol-2-one | HCID 22754947 | — |
| Reactant | HCID 46208786 | HCID 46208786 | — |
| Product | HCID 67391805 | HCID 67391805 | — |
Reaction Steps
Compound 55 was prepared by the general procedure for compound 1, by using compound A-10 and 5-aminobenzimidazolone as starting materials (5-aminobenzimidazolone was prepared by reduction of 5-nitrobenzimidazolone according to Regan, J. and coll. J. Med. Chem. 2002, 45, 2994-3008). 1H NMR (500 MHz, DMSO-d6) δ 10.67 (s, 1H), 10.60 (s, 1H), 10.01 (s, 1H), 7.42 (s, 1H), 7.17 (br d, 1H, J=8.2 Hz), 6.89 (d, 1H, J=8.5 Hz), 4.10 (m, 2H), 3.04 (br t, 1H, J=12.5 Hz), 2.74 (m, 1H), 1.77 (m, 2H), 1.67 (m, 1H), 1.53 (m, 1H), 1.15 (m, 1H), 0.93 (d, 3H, J=6.6 Hz). MS (M+1): 410.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716312B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-194778d198c14f64aa59eb7db2f2f504 |
| Source note | uspto-grants-2014_05 |