2-Chloro-5-methylbenzoic Acid → HCID 73673436, compound

HRID 1482501Notes

Reaction equation

HRID 1482501 reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:3]=1[C:4]([OH:6])=O.[N:12]1([CH:18]([C:21]2[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=2)[CH2:19][NH2:20])[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1>>[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:3]=1[C:4]([NH:20][CH2:19][CH:18]([N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)[C:21]1[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=1)=[O:6]

Participants

3

Reactant 2

HCID 2404302-Chloro-5-methylbenzoic AcidHCID 49889912-Morpholin-4-yl-2-(3-pyridyl)ethylamine

Product 1

HCID 73673436HCID 73673436, compound

Procedure

From 2-chloro-5-methylbenzoic acid and (2-morpholin-4-yl-2-pyridin-3-ylethyl)amine. LCMS (MH+): m/z=360.0, tR (minutes, Method A)=0.77

Sources & evidence

ORD record
ord-27b8585ef1944922bf2c23328f92b503
Source dataset
uspto-grants-2016_08
Patent number
US09415055B2

Reaction notes

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