HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-6-methylpyridine → 1,2-difluoro-3-isothiocyanatobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-6-methylpyridine | HCID 15765 | — |
| Reactant | 2,3-Difluoroaniline | HCID 78278 | — |
| Reactant | HCID 64628889 | HCID 64628889 | — |
| Product | 1,2-difluoro-3-isothiocyanatobenzene | HCID 2758330 | — |
Reaction Steps
The title compound, MS (ISP): m/e=347.3 (M+H+), was prepared as for example 1, steps A to C. Step A was performed using 1,2-difluoro-3-isothiocyanato-benzene and yielded 5-(2,3-difluoro-phenylamino)-thiazole-4-carboxylic acid ethyl ester. This was hydrolized in step B to 5-(2,3-difluoro-phenylamino)-thiazole-4-carboxylic acid, which was reacted with 6-methyl-pyridin-2-ylamine in step C. 1,2-Difluoro-3-isothiocyanato-benzene was prepared as in example 96, starting from 2,3-difluoro-phenylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678815B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-a4cf498a233e4a4fb7dd6befddfb915f |
| Source note | uspto-grants-2010_03 |