Methyl 3-bromopropanoate → HCID 86709302, compound

HRID 1478388Notes

Reaction equation

HRID 1478388 reaction equation
[CH3:1][O:2]C(=O)CCBr.[CH3:8][Si:9]([CH3:39])([CH3:38])[CH2:10][CH2:11][O:12][CH2:13][N:14]1[C:18]([C:19]2[CH:37]=[CH:36][C:22]([O:23][C:24]3[CH:25]=[C:26]4[C:30](=[CH:31][CH:32]=3)[N:29]([CH2:33][CH2:34]O)[N:28]=[CH:27]4)=[CH:21][CH:20]=2)=[CH:17][CH:16]=[N:15]1>>[CH3:39][Si:9]([CH3:38])([CH3:8])[CH2:10][CH2:11][O:12][CH2:13][N:14]1[C:18]([C:19]2[CH:20]=[CH:21][C:22]([O:23][C:24]3[CH:25]=[C:26]4[C:30](=[CH:31][CH:32]=3)[N:29]([CH2:33][CH2:34][CH2:1][OH:2])[N:28]=[CH:27]4)=[CH:36][CH:37]=2)=[CH:17][CH:16]=[N:15]1

Participants

3

Reactant 2

HCID 76934Methyl 3-bromopropanoateHCID 86709303HCID 86709303, compound

Product 1

HCID 86709302HCID 86709302, compound

Procedure

The titled compound AA is synthesized from intermediate Y-1 and 3-bromo-propionic acid methyl ester according to the procedure described for the synthesis of intermediate Y.

Sources & evidence

ORD record
ord-2a00b134c5b947ed91bab74688ad9ca0
Source dataset
uspto-grants-2016_08
Patent number
US09403830B2

Reaction notes

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