Ethyl 3-hydroxy-2-nitrobutanoate → HCID 54371401, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[N:7]=[CH:8][C:9]2[NH:10][C:11]3[C:16]([C:17]=2[C:18]=1[CH3:19])=[C:15]([CH2:20][OH:21])[CH:14]=[CH:13][CH:12]=3)=[O:5])[CH3:2].C(OC(=O)C([N+]([O-])=O)C(O)C)C>>[CH2:1]([O:3][C:4]([C:6]1[N:7]=[CH:8][C:9]2[NH:10][C:11]3[C:16]([C:17]=2[C:18]=1[CH3:19])=[C:15]([CH:20]=[O:21])[CH:14]=[CH:13][CH:12]=3)=[O:5])[CH3:2]Participants
3
Procedure
The synthesis takes place according to the method described in example 1 from 5-hydroxymethyl-4-methyl-beta-carboline-3-carboxylic acid ethyl ester, which in turn is prepared according to example 2 from 2-nitro-3-hydroxybutyric acid ethyl ester in 5 stages.
Workup
- customis prepared
Sources & evidence
- ORD record
- ord-0c6dedb474a14471bb70bde7e54ffb97
- Source dataset
- uspto-grants-1988_07
- Patent number
- US04757070
Reaction notes
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