HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenylhydrazine hydrochloride → 8-Bromo-5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Reactant | 1-Oxo-indan-4-carboxylic acid | HCID 12542206 | — |
| Product | 8-Bromo-5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acid | HCID 22462803 | — |
Reaction Steps
In a manner similar to Example 17, 1-oxo-indan-4-carboxylic acid and 4-bromophenylhydrazine hydrochloride were reacted to form 8-bromo-5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acid which was converted to the ethyl ester in a manner similar to that described in Example 22 to afford the title compound as a tan solid: mp 198-200° C.; 1H NMR (DMSO-d6): δ 1.39 (t, 3H), 4.00 (s, 2H), 4.37 (q, 2H), 7.22 (d, 1H), 7.42 (d, 1H), 7.52 (t, 1H), 7.79-7.84 (m, 3H), 11.86 (s, 1H); MS [EI, m/z]: 355 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06391902B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-655085f22b2e4be1af0f2d7fa322c12e |
| Source note | uspto-grants-2002_05 |