HCID 53302654, compound → HCID 70975385, compound

HRID 404010Notes

Reaction equation

HRID 404010 reaction equation
ClC1C=CC=CC=1NC(=O)NC1C=CC(C2C=C3C(CN([C@@H](C(C)C)C(O)=O)C3=O)=CC=2)=NC=1.[CH2:35]1[C:43]2[C:38](=[CH:39][C:40]([NH:44][C:45](=[O:72])[NH:46][C:47]3[CH:52]=[CH:51][C:50]([C:53]4[CH:61]=[C:60]5[C:56]([CH2:57][N:58]([C@@H:63]([CH:68]([CH3:70])[CH3:69])[C:64]([O:66]C)=[O:65])[C:59]5=[O:62])=[CH:55][CH:54]=4)=[CH:49][C:48]=3[F:71])=[CH:41][CH:42]=2)[CH2:37][CH2:36]1>>[CH2:35]1[C:43]2[C:38](=[CH:39][C:40]([NH:44][C:45](=[O:72])[NH:46][C:47]3[CH:52]=[CH:51][C:50]([C:53]4[CH:61]=[C:60]5[C:56]([CH2:57][N:58]([C@@H:63]([CH:68]([CH3:69])[CH3:70])[C:64]([OH:66])=[O:65])[C:59]5=[O:62])=[CH:55][CH:54]=4)=[CH:49][C:48]=3[F:71])=[CH:41][CH:42]=2)[CH2:37][CH2:36]1

Participants

3

Reactant 2

HCID 53302654HCID 53302654, compoundHCID 70975553(S)-2-(6-(5-(3-(2-Chlorophenyl)ureido)pyridin-2-yl)-1-oxoisoindolin-2-yl)-3-methylbutanoic acid

Product 1

HCID 70975385HCID 70975385, compoundYield 82%

Procedure

The compound of example 438 was prepared analogous to the compound of example 394 by hydrolysis of the compound of example 437.

Sources & evidence

ORD record
ord-4653df026b1e44909cc81deaaae35c05
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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