HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23433467, compound → HCID 22279055, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23433467 | HCID 23433467 | — |
| Reactant | HCID 23433515 | HCID 23433515 | — |
| Product | HCID 22279055 | HCID 22279055 | 99% |
Reaction Steps
This compound was prepared from 6-tert-butyloxycarbamoyl-2-nitrotoluene (4.60 g, 18.2 mmol) in a manner similar to that described for 3-tert-butyloxycarbamoylaniline (EXAMPLE 147), affording 4.00 g (99%) of 2-amino-6-tert-butyloxycarbamoyltoluene as a colorless oil. Data for 2-amino-6-tert-butyloxycarbamoyltoluene: 1H NMR (400 MHz, CDCl3) 7.04 (br d of ABq, JAB =8.0, JA =0, JB =7.9, 2H, 5,4-H), 6.49 (d, J=8.3, 1H. 3-H), 6.26 (br s, 1H, NH), 3.61 (br s, 2H, NH2), 2.02 (s, 3H, 1-CH3), 1.51 [s, 9H, (CH3)3CO)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05696127 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-22cc9ed619a843769078b9d1f6ecd5f3 |
| Source note | uspto-grants-1997_12 |