3-Hydroxypropionic acid → HCID 178520900, compound

HRID 1260750Notes

Reaction equation

HRID 1260750 reaction equation
Cl.Cl.Cl.[O:4]1[C:8]2=[C:9]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH2:27])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[N:10]=[CH:11][CH:12]=[C:7]2[CH2:6][CH2:5]1.[OH:28][CH2:29][CH2:30][C:31](O)=[O:32]>>[O:4]1[C:8]2=[C:9]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH:27][C:29](=[O:28])[CH2:30][CH2:31][OH:32])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[N:10]=[CH:11][CH:12]=[C:7]2[CH2:6][CH2:5]1

Participants

3

Reactant 2

HCID 681523-Hydroxypropionic acidHCID 178478590HCID 178478590, compound2×

Product 1

HCID 178520900HCID 178520900, compound

Procedure

The title compound, white solid (99 mg, 98%), MS (ISP) m/z=403.5 [(M+H)+], mp 257° C., was prepared in accordance with the general method of example 6 from trans-4-{2-[4-(2,3-dihydro-furo[2,3-c]pyridin-7-yl)-piperazin-1-yl]-ethyl}-cyclohexylamine trihydrochloride (intermediate B) (110 mg, 0.25 mmol) and 3-hydroxy-propionic acid.

Sources & evidence

ORD record
ord-0564d6757cce4966b07a59d832b1fc07
Source dataset
uspto-grants-2013_06
Patent number
US08470828B2

Reaction notes

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