HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivalaldehyde → 1,1-Dimethylethyl (3S)-3-[(3-chloro-4-cyanophenyl)amino]-4-[(2,2-dimethylpropyl)amino]butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1,1-Dimethylethyl (3S)-4-amino-3-[(3-chloro-4-cyanophenyl)amino]butanoate | HCID 59516153 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1-Dimethylethyl (3S)-3-[(3-chloro-4-cyanophenyl)amino]-4-[(2,2-dimethylpropyl)amino]butanoate | HCID 59516168 | 98% |
Reaction Steps
NaBH(OAc)3 (0.5 g, 2.32 mmol) was added to a solution of 1,1-dimethylethyl (3S)-4-amino-3-[(3-chloro-4-cyanophenyl)amino]butanoate (0.48 g, 1.55 mol), and trimethylacetaldehyde (0.14 g, 1.60 mmol) in CH2Cl2 (35 mL). After stirring at room temperature for 2 h, the reaction was diluted with CH2Cl2 (35 mL), washed with saturated NaHCO3, dried over Na2SO4, filtered, and concentrated to yield the titled product (0.575 g, 98%) as an oil. LC-MS (ES) m/e 380.6 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816395B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-7f2788a5bdaf4e9e96c7d56d59de37b7 |
| Source note | uspto-grants-2010_10 |