Hydrochloric Acid → HCID 67395342, compound
Reaction equation
C([S@@]([NH:7][C@@H:8]([C:10]1[S:14][C:13]([C:15]([O-:17])=[O:16])=[CH:12][CH:11]=1)[CH3:9])=O)(C)(C)C.[ClH:18]>>[ClH:18].[NH2:7][C@@H:8]([C:10]1[S:14][C:13]([C:15]([OH:17])=[O:16])=[CH:12][CH:11]=1)[CH3:9]Participants
3
Conditions
- Temperature
- 60 °C
Procedure
To a vial containing 5-[(1R)-1-{[(S)-tert-butylsulfinyl]amino}ethyl]thiophene-2-carboxylate (0.050 g, 0.15 mmol) was added hydrochloric acid (3 mL, 12.0 mmol, 4.0 M of in 1,4-dioxane). This mixture was capped and heated at 60° C. for 2 h, after which it was evaporated to dryness to afford (R)-5-(1-aminoethyl)thiophene-2-carboxylic acid hydrochloride as a white solid. LC-MS: (FA) ES+ 172.
Workup
- customThis mixture was capped
- customafter which it was evaporated to dryness
Sources & evidence
- ORD record
- ord-e75f399889d14fa2879570252ef3876c
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08546588B2
Reaction notes
Loading…