5-Amino-5-oxopentanoic acid → HCID 60142841, compound

HRID 2176776Notes

Reaction equation

HRID 2176776 reaction equation
[CH3:1][O:2][C:3]([N:5]1[C@@H:13]2[C@@H:8]([C@@:9]([OH:23])([C:14]#[C:15][C:16]3[CH:17]=[C:18]([CH3:22])[CH:19]=[CH:20][CH:21]=3)[CH2:10][CH2:11][CH2:12]2)[CH2:7][CH2:6]1)=[O:4].[C:24]([CH2:27][CH2:28][CH2:29][C:30](O)=[O:31])(=[O:26])[NH2:25]>>[NH2:25][C:24](=[O:26])[CH2:27][CH2:28][CH2:29][C:30]([O:23][C@@:9]1([C:14]#[C:15][C:16]2[CH:17]=[C:18]([CH3:22])[CH:19]=[CH:20][CH:21]=2)[CH2:10][CH2:11][CH2:12][C@@H:13]2[C@H:8]1[CH2:7][CH2:6][N:5]2[C:3]([O:2][CH3:1])=[O:4])=[O:31]

Participants

3

Reactant 2

HCID 1683565-Amino-5-oxopentanoic acidHCID 68276168(3aS,4R,7aS)-4-hydroxy-4-m-tolylethynyl-octahydro-indole-1-carboxylic acid methyl ester

Product 1

HCID 60142841HCID 60142841, compound

Procedure

Synthesis in analogy to the General Method 1 starting from (3aS,4R,7aS)-4-hydroxy-4-m-tolylethyny-octahydro-indole-1-carboxylic acid methyl ester and 4-carbamoyl-butyric acid to yield (3aR,4S,7aR)-methyl 4-(5-amino-5-oxopentanoyloxy)-4-(m-tolylethynyl)octahydro-1H-indole-1-carboxylate. MS [M+H]=427; RT=1.01 min; UPLC Method I

Sources & evidence

ORD record
ord-317803d0bb4e47f18e618b7c7d43c30a
Source dataset
uspto-grants-2015_06
Patent number
US09067881B2

Reaction notes

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