HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-[2-Acetamido-4-dimethylaminophenyl]-3-(1-ethyl-2-methyl-3-indolyl)-4,5,6,7-tetrachlorophthalide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N,N-dimethyl-m-phenylenediamine | HCID 76084 | — |
| Reactant | 1-Ethyl-2-methyl-3-(2-carboxy-3,4,5,6-tetrachlorobenzoyl)indole | HCID 19763805 | — |
| Product | 3-[2-Acetamido-4-dimethylaminophenyl]-3-(1-ethyl-2-methyl-3-indolyl)-4,5,6,7-tetrachlorophthalide | HCID 20523548 | — |
Reaction Steps
Proceeding in a manner similar to that described in Example 13 above, 4.43 g (0.01 mole) of 2-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-3,4,5,6-tetrachlorobenzoic acid, prepared as described in Example 2, part A above, was interacted with 2.0 g (0.015 mole) of m-amino-N,N-dimethylaniline in the presence of ten ml of acetic anhydride to obtain 3-[2-acetamido-4-dimethylaminophenyl]-3-(1-ethyl-2-methyl-3-indolyl)-4,5,6,7-tetrachlorophthalide (Formula III: R°=R1 =R2 =R3 =Cl; R=R5 =CH3 ; ##STR34## R6 =CH2CH3 ; Y1H) which developed a blue-green color when spotted on silica gel in the form of a toluene solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04322352 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-9569116ca3ed4f638a58f7e83d9e5073 |
| Source note | uspto-grants-1982_03 |