Methyl 3-bromopropanoate → HCID 86709304, compound

HRID 1478389Notes

Reaction equation

HRID 1478389 reaction equation
C[O:2][C:3](=O)[CH2:4][CH2:5]Br.[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](CCO)[N:28]=[CH:27]4)=[CH:21][CH:20]=2)=[CH:17][CH:16]=[N:15]1>>[CH3:38][Si:9]([CH3:39])([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:32]=[CH:31][C:30]4[C:26](=[CH:27][N:28]([CH2:5][CH2:4][CH2:3][OH:2])[N:29]=4)[CH:25]=3)=[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 86709304HCID 86709304, compound

Procedure

The titled compound AB 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-02648508588c4429bf11a26d289fdb99
Source dataset
uspto-grants-2016_08
Patent number
US09403830B2

Reaction notes

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