HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloroacetylpyridine → (1S)-2-(methylamino)-1-pyridin-3-ylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloroacetylpyridine | HCID 416252 | — |
| Reactant | (R)-2-(methylamino)-1-pyridin-2-ylethanol | HCID 10149007 | — |
| Product | (1S)-2-(methylamino)-1-pyridin-3-ylethanol | HCID 10171254 | — |
Reaction Steps
As described for the preparation of (1R)-2-(methylamino)-1-pyridin-2-ylethanol (Preparations 68-69), 3-chloroacetylpyridine (Chem. Ber. 1951, 84, 147-149) is converted to the title compound, isolated as a pale yellow amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852731B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-6c954c04dc1b4bf78b7a007ae0df0223 |
| Source note | uspto-grants-2005_02 |