HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67531620, compound → HCID 67531311, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67531620 | HCID 67531620 | — |
| Reactant | HCID 67531839 | HCID 67531839 | — |
| Product | HCID 67531311 | HCID 67531311 | 85% |
Reaction Steps
Following the same procedure to synthesize 2-(2-amino-1H-benzo[d]imidazol-6-ylcarbamoyl)benzoic acid hydrochloride, tert-butyl 6-amino-2-(bis(tert-butoxycarbonyl)amino)-1H-benzo[d]imidazole-1-carboxylate (0.167 g, 0.372 mmol) was reacted with (S)-7-oxaspiro[3.5]nonane-6,8-dione (0.057 g, 0.372 mmol) to give the title product (0.107 g, 85% yield) as a yellow solid. 1H NMR (300 MHz, CD3OD) δ 7.49 (s, 1H), δ 6.95 (s, 2H), δ 2.24 (m, 4H), δ 1.32 (m, 8H) ppm; 13C NMR (75 MHz, CD3OD) δ 175.2, 173.8, 171.8, 151.9, 135.0, 129.7, 116.7, 111.3, 103.9, 44.4, 43.9, 42.0, 39.7, 37.8, 24.1 ppm; HRMS (ESI) Calcd for C15H18N4O3(M+) 302.1379. Found 302.1373.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221765B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-61bf66196391440da7c3fc725e7b6bb5 |
| Source note | uspto-grants-2015_12 |