Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279950Generated: November 1, 2026

HCID 23433467, compound → HCID 22279055, compound

https://huagongshe.com/reaction/1279950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23433467HCID 23433467—
ReactantHCID 23433515HCID 23433515—
ProductHCID 22279055HCID 2227905599%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448405B1
Source datasetuspto-grants-2002_09
ORD IDord-5abb83b7f70f417f8fdc5df6ee79830e
Source noteuspto-grants-2002_09