Methane → HCID 70507384, compound
Reaction equation
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][C:11]([OH:13])=[O:12])[CH2:6][CH2:5]1)(=[NH:3])[NH2:2].C.[ClH:15]>>[ClH:15].[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][C:11]([OH:13])=[O:12])[CH2:6][CH2:5]1)(=[NH:2])[NH2:3]Participants
4
Procedure
11.5 g of 1-amidino-4-piperidineacetic acid prepared in Example 54 was dissolved in 100 ml of a 1 N hydrochloric acid solution, and the solution was treated with activated charcoal and concentrated. Acetone was added to the residue to obtain 12.7 g (yield: 92%) of 1-amidino-4-piperidineacetic acid hydrochloride as colorless prisms having a melting point of 213° to 215.5° C.
Workup
- concentrationconcentrated
- additionAcetone was added to the residue
Sources & evidence
- ORD record
- ord-c8e669ab704740b087b53ced628a2ab7
- Source dataset
- uspto-grants-1984_02
- Patent number
- US04433152
Reaction notes
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