Methyl 3-amino-2-methylpropanoate hydrochloride → Methyl 1-(aminomethyl)cyclopropane-1-carboxylate--hydrogen chloride (1/1)

HRID 590564Notes

Reaction equation

HRID 590564 reaction equation
[ClH:1].[NH2:2][CH2:3][CH:4]([CH3:9])[C:5]([O:7][CH3:8])=[O:6].N[CH2:11]C1(C(O)=O)CC1>>[ClH:1].[NH2:2][CH2:3][C:4]1([C:5]([O:7][CH3:8])=[O:6])[CH2:11][CH2:9]1

Participants

3

Reactant 2

HCID 13063725Methyl 3-amino-2-methylpropanoate hydrochlorideHCID 150339011-(Aminomethyl)cyclopropanecarboxylic acid

Product 1

HCID 21464884Methyl 1-(aminomethyl)cyclopropane-1-carboxylate--hydrogen chloride (1/1)

Procedure

The title compound was prepared in analogy to Compound W in Example 20 by using 1-(aminomethyl)cyclopropanecarboxylic acid (CAS number: 139132-50-6, J&K; for its synthesis, please refer to: Mertin A., et al. Synlett, 1991, 2, 87-9) instead of DL-3-aminoisobutyric acid.

Sources & evidence

ORD record
ord-371ed32666a142eca0c49046322d6718
Source dataset
uspto-grants-2016_01
Patent number
US09233978B2

Reaction notes

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