HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl [4-(2-aminoethyl)pyridin-2-yl]carbamate → HCID 67243361, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl [4-(2-aminoethyl)pyridin-2-yl]carbamate | HCID 22097761 | — |
| Reactant | HCID 63761213 | HCID 63761213 | — |
| Reactant | 4-Chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide | HCID 67243160 | — |
| Reactant | HCID 86625884 | HCID 86625884 | — |
| Product | HCID 67243361 | HCID 67243361 | — |
| Product | HCID 86625884 | HCID 86625884 | — |
Reaction Steps
The title compound was prepared in two steps. tert-Butyl (4-{2-[(2-isopropyl-1,1-dioxido-3-oxo-5-phenyl-2,3-dihydroisothiazol-4-yl)amino]ethyl}pyridin-2-yl)carbamate was prepared from 4-chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide and tert-butyl [4-(2-aminoethyl)pyridin-2-yl]carbamate in a similar manner as described for Example 118. Deprotection of tert-butyl (4-{2-[(2-isopropyl-1,1-dioxido-3-oxo-5-phenyl-2,3-dihydroisothiazol-4-yl)amino]ethyl}pyridin-2-yl)carbamate in a similar manner as described for 1-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]azetidin-3-amine gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723333B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-ca3bf0537bee4813b8660b4d16ce59fe |
| Source note | uspto-grants-2010_05 |