HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10023113, compound → HCID 57205166, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10023113 | HCID 10023113 | — |
| Reactant | HCID 21355906 | HCID 21355906 | — |
| Product | HCID 57205166 | HCID 57205166 | — |
Reaction Steps
The title compound was prepared as described in the example for the synthesis of the enantiomer, (1R,2R)-2-methyl-1-phenyl-1,3-propanediamine, from methyl (2R,3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-2-methyl-3-phenylpropionate (Davies et al., J. Chem. Soc. Chem. Commun. 1153-1155, 1993). The title compound was obtained as a crystallizing oil, MS (m/z): 165.3 (M+H)+; C10H16N2 requir. 164.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921762B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-31c77135d15042368464147f21ecfb33 |
| Source note | uspto-grants-2005_07 |