HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703208Generated: October 26, 2026
1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl- → 3-[2,4-Bis(dimethylamino)phenyl]-3-(1-ethyl-2-methyl-3-indolyl)-6-nitrophthalide
https://huagongshe.com/reaction/1703208
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Benzenediamine, N1,N1,N3,N3-tetramethyl- | HCID 89715 | — |
| Reactant | 2-(1-Ethyl-2-methyl-1H-indole-3-carbonyl)-5-nitrobenzoic acid | HCID 20523561 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 3-[2,4-Bis(dimethylamino)phenyl]-3-(1-ethyl-2-methyl-3-indolyl)-6-nitrophthalide | HCID 20523544 | 76.2% |
Reaction Steps
A mixture of 3.68 g (0.01 mole) of 2-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-5-nitrobenzoic acid, prepared as described in part A above, and 2.0 g (0.012 mole) of N,N,N',N'-tetramethyl-m-phenylenediamine in 10.0 ml of acetic anhydride was heated at 90° C. for one hour and then allowed to cool to 25° C. The solid which separated was collected by filtration, washed with diethylether and dried to obtain 3.8 g of 3-[2,4-bis(dimethylamino)phenyl]-3-(1-ethyl-2-methyl-3-indolyl)-6-nitrophthalide (Formula III: R0 =R1 =R3 =Y1 =H; R2 =NO2 ; R=R5 =CH3 ; R4 =N(CH3)2 ; R6 =CH2CH3) as an orange solid which melted over the range 185°-187° C. The nuclear magnetic resonance spectrum was in accord with the assigned structure. A benzene solution of this product developed a black-purple color when spotted on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04351768 |
|---|
| Source dataset | uspto-grants-1982_09 |
|---|
| ORD ID | ord-1ad5250738d94f658e5bae4eb308918d |
|---|
| Source note | uspto-grants-1982_09 |
|---|