2-Morpholinoethylamine → HCID 67279861, compound

HRID 1692633Notes

Reaction equation

[CH2:1]([O:5][C:6]([C:8]1[C:18]2[O:17][C:16]3[C:19]([CH:25]=O)=[C:20]([OH:24])[CH:21]=[C:22]([CH3:23])[C:15]=3[C:14](=[O:27])[O:13][C:12]=2[C:11]([CH3:28])=[C:10]([O:29][CH3:30])[CH:9]=1)=[O:7])[CH2:2][CH2:3]C.[N:31]1([CH2:37][CH2:38][NH2:39])[CH2:36][CH2:35][O:34][CH2:33][CH2:32]1>>[CH2:1]([O:5][C:6]([C:8]1[C:18]2[O:17][C:16]3[C:19]([CH2:25][NH:39][CH2:38][CH2:37][N:31]4[CH2:36][CH2:35][O:34][CH2:33][CH2:32]4)=[C:20]([OH:24])[CH:21]=[C:22]([CH3:23])[C:15]=3[C:14](=[O:27])[O:13][C:12]=2[C:11]([CH3:28])=[C:10]([O:29][CH3:30])[CH:9]=1)=[O:7])[CH2:2][CH3:3]

Participants

Reactant 2

HCID 4082852-Morpholinoethylamine

HCID 86643253HCID 86643253, compound

Product 1

HCID 67279861HCID 67279861, compound

Procedure

This compound was prepared from the compound from Example 8 by means of a procedure similar to that used for Example 18 except replacing ethanolamine with 2-morpholin-4-yl-ethylamine.

Sources & evidence

ORD record: ord-9695b6a71740472aab156decd3f1e3da
Source dataset: uspto-grants-2012_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08158623B2

Reaction notes

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