HCID 16244268, compound → 2-(2-{3-[4-(3,4-Difluoro-phenoxy)-piperidin-1-yl]-2-hydroxy-propoxy}-benzoylamino)-2-methyl-propionic Acid Methyl Ester

HRID 496186Notes

Reaction equation

[F:1][C:2]1[CH:3]=[C:4]([CH:12]=[CH:13][C:14]=1[F:15])[O:5][CH:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1.[CH3:16][C:17]([NH:23][C:24](=[O:36])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[O:31][CH2:32][CH:33]1[CH2:35][O:34]1)([CH3:22])[C:18]([O:20][CH3:21])=[O:19]>C1(C)C=CC=CC=1.CO>[CH3:21][O:20][C:18](=[O:19])[C:17]([NH:23][C:24](=[O:36])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[O:31][CH2:32][CH:33]([OH:34])[CH2:35][N:9]1[CH2:10][CH2:11][CH:6]([O:5][C:4]2[CH:12]=[CH:13][C:14]([F:15])=[C:2]([F:1])[CH:3]=2)[CH2:7][CH2:8]1)([CH3:16])[CH3:22]

Participants

Conditions

Temperature: 100 °C

Procedure

A toluene solution of 4-(3,4-difluorophenoxy)piperidine (0.03 ml, 0.5 M) was mixed with a toluene solution of methyl 2-methyl-2-{[2-(2-oxiranylmethoxy)benzoyl]amino}-propanoate (0.03 ml, 0.5 M). The mixture was diluted with 0.20 ml toluene and 0.05 ml methanol. The reaction mixture was stirred overnight at 100° C. in sealed vials. The product were concentrated in vacuo and used without any purification.

Workup

concentrationThe product were concentrated in vacuo
customused without any purification

Sources & evidence

ORD record: ord-884f934e07f84bf0ae34a26fc607b3c4
Source dataset: uspto-grants-2005_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06943188B2

Reaction notes

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