HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510187Generated: October 30, 2026
Dimethyl Sulfoxide → tert-butyl (2R)-2-[(6-chloropyrazin-2-yl)amino]propanoate
https://huagongshe.com/reaction/510187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 2,6-Dichloropyrazine | HCID 78504 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | D-Alanine tert-butyl ester hydrochloride | HCID 16211919 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-butyl (2R)-2-[(6-chloropyrazin-2-yl)amino]propanoate | HCID 117639895 | — |
Reaction Steps
To a reaction vessel was added 2,6-dichloropyrazine (CA, 492 mg, 3.30 mmol), D-Alanine tert-butyl ester hydrochloride (Aldrich Chemical) (500 mg, 2.75 mmol), DMSO (3 mL) and DIPEA (1.923 mL, 11.01 mmol). The resulting solution was heated to 120° C. for 18 hrs. The reaction mixture was cooled and diluted with ethyl acetate (30 mL). The organic layer was washed with aqueous sodium hydrogen carbonate followed by aq. brine. The aqueous layers were back extracted with ethyl acetate and the combined organic layers dried with sodium sulfate, filtered and concentrated to give an oil. The residue was purified by silica gel chromatography on Biotage 50 g SNAP column, eluting with EtOAc/Hexane (10-60%) to give the product, I-9, as a yellow oil. (663 mg, 93%) LRMS (ESI) m/z 258.1 [(M+H)+; calcd for C11H16ClN3O2: 258.1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096598B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-03b90a0008384bc4902bf7f67259f55a |
|---|
| Source note | uspto-grants-2015_08 |
|---|