HCID 53802369, compound → HCID 54142299, compound

HRID 429220Notes

Reaction equation

HRID 429220 reaction equation
[CH2:1](OC(N[C@](CC)(C(O)=O)CCC(O)=O)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O:30][C:31]([NH:33][C@:34]([CH2:43][CH2:44][CH3:45])([C:40]([OH:42])=[O:41])[CH2:35][CH2:36][C:37](O)=[O:38])=O)C1C=CC=CC=1>>[CH2:1]([C:31]([NH:33][C@:34]1([CH2:43][CH3:44])[C:40](=[O:42])[O:41][C:37](=[O:38])[CH2:36][CH2:35]1)=[O:30])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1.[CH2:1]([C:31]([NH:33][C@:34]1([CH2:43][CH2:44][CH3:45])[C:40](=[O:42])[O:41][C:37](=[O:38])[CH2:36][CH2:35]1)=[O:30])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 2

HCID 53802369HCID 53802369, compoundHCID 54554922HCID 54554922, compound

Product 2

HCID 54142299HCID 54142299, compoundHCID 54333898HCID 54333898, compound

Procedure

In a similar fashion from N-benzyloxycarbonyl-α-ethylglutamic acid and N-benzyloxycarbonyl-α-propylglutamic acid. there is obtained N-benzylcarbonyl-α-ethylglutamic anhydride and N-benzylcarbonyl-α-propylglutamic anhydride, respectively.

Sources & evidence

ORD record
ord-2ea429f40eb245bbbdedabf58b6620a6
Source dataset
uspto-grants-2001_11
Patent number
US06316471B1

Reaction notes

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