HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,4-Trimethyl-1,2-dihydroquinolin-7-amine → HCID 10631958, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,4-Trimethyl-1,2-dihydroquinolin-7-amine | HCID 281792 | — |
| Reactant | HCID 23433536 | HCID 23433536 | — |
| Product | HCID 10631958 | HCID 10631958 | — |
Reaction Steps
Removal of the Boc protective group of 7-tert-butyloxycarbamoyl-1,2-dihydro-2,2,4,8-tetramethylquinoline (400 mg, 1.32 mmol) was effected in the manner similar to that described for 7-amino-1,2-dihydro-2,2,4-trimethylquinoline (EXAMPLE 13), affording 267 mg (quantitative) of the desired aniline as a light reddish oil. Data for 7-amino-1,2-dihydro-2,2,4,8-tetramethylquinoline: 1H NMR (400 MHz, CDCl3) 6.82 (d, 1H, J=8.2 Hz, 5-H), 6.08 (d, 1H, J=8.1 Hz, 6-H), 5.15 (d, 1H, J=1.2 Hz, 3-H), 3.56 (br s, 3H, NH2, NH), 1.95 (d, 3H, J=1.2 Hz, 4-CH3), 1.91 (s, 3H, 8-CH3), 1.27 [s, 6H, 2-(CH3)2 ].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06017924 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-ed69b89ad04f4f3299ca7eedc459ef9b |
| Source note | uspto-grants-2000_01 |