Tetrahydrofuran → N-[4-(4-Hydroxy-3-isopropyl-phenoxy)-3,5-dimethyl-phenyl]-malonamic acid methyl ester

HRID 1270575Notes

Reaction equation

[NH2:1][C:2]1[CH:18]=[C:17]([CH3:19])[C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[C:9]([CH:14]([CH3:16])[CH3:15])[CH:8]=2)=[C:4]([CH3:20])[CH:3]=1.C(N(CC)CC)C.C[CH:29]([C:33](Cl)=[O:34])[C:30](Cl)=[O:31].C1C[O:39][CH2:38]C1>>[CH3:38][O:39][C:33](=[O:34])[CH2:29][C:30]([NH:1][C:2]1[CH:3]=[C:4]([CH3:20])[C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[C:9]([CH:14]([CH3:16])[CH3:15])[CH:8]=2)=[C:17]([CH3:19])[CH:18]=1)=[O:31]

Participants

Reactant 4

HCID 8028Tetrahydrofuran

HCID 8471Triethylamine

HCID 10931669Methylmalonylchloride

HCID 121141794-(4-Amino-2,6-dimethyl-phenoxy)-2-isopropyl-phenol

Product 1

HCID 12114180N-[4-(4-Hydroxy-3-isopropyl-phenoxy)-3,5-dimethyl-phenyl]-malonamic acid methyl ester

Procedure

To a solution of 4-(4-amino-2,6-dimethyl-phenoxy)-2-isopropyl-phenol (39 mg, 0.14 mmol) in THF (2 mL) was added triethylamine (22 μL, 0.16 mmol) and methyl malonyl chloride (16 μL, 0.15 mmol). The resulting mixture was stirred at RT for 18 h. The solution was concentrated and the residue was purified by preparative TLC (2.5% MeOH in CH2Cl2) to give the title compound of Step D (31 mg). MS (APCI−) Calc.: 371.3, Found: 370.3 (M−1).

Workup

concentrationThe solution was concentrated
customthe residue was purified by preparative TLC (2.5% MeOH in CH2Cl2)

Sources & evidence

ORD record: ord-5c03ddf7c9214d948e8faaa860234ff6
Source dataset: uspto-grants-2007_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07202275B2

Reaction notes

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