HCID 12773658, compound → HCID 20340037, compound

HRID 1395595Notes

Reaction equation

HRID 1395595 reaction equation
[C:1]([CH2:4][CH2:5][CH2:6][CH:7]=[CH:8][CH2:9][CH:10]1[N:14]([CH2:15][CH2:16][CH:17]([OH:23])[CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[C:13](=[O:24])[NH:12][C:11]1=[O:25])([OH:3])=[O:2].C(CCCCCCC1N(CCC(O)CCCCC)C(=O)NC1=O)(O)=O>>[C:1]([CH2:4][CH2:5][CH2:6][C:7]#[C:8][CH2:9][CH:10]1[N:14]([CH2:15][CH2:16][CH:17]([OH:23])[CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[C:13](=[O:24])[NH:12][C:11]1=[O:25])([OH:3])=[O:2]

Participants

3

Reactant 2

HCID 12773658HCID 12773658, compoundHCID 70510127HCID 70510127, compound

Product 1

HCID 20340037HCID 20340037, compound

Procedure

This compound was then catalytically hydrogenated to the corresponding 5-(6-carboxyhex-2-enyl)-1-(3-hydroxyoctyl) hydantoin and subsequently to the corresponding saturated compound which was found to be identical with the title compound of Example 2.

Sources & evidence

ORD record
ord-13488bb312494e359a3c08c0828e9db7
Source dataset
uspto-grants-1980_05
Patent number
US04204068

Reaction notes

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