Benzoic Acid → HCID 24798586, compound
Reaction equation
[NH:1]([CH2:3][C:4]([OH:6])=[O:5])[CH3:2].Cl[Si](C)(C)C.CCN([CH:18]([CH3:20])[CH3:19])C(C)C.Cl[C:22]([O:24][CH:25](Cl)[CH:26]([CH3:28])[CH3:27])=[O:23].[C:30]([OH:38])(=[O:37])[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1>C(Cl)(Cl)Cl>[CH3:2][N:1]([C:22]([O:24][CH:25]([C:26]1[CH:28]=[CH:19][CH:18]=[CH:20][CH:27]=1)[O:38][C:30]([C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:37])=[O:23])[CH2:3][C:4]([OH:6])=[O:5]Participants
7
Procedure
Following the general procedure for the one pot synthesis, sarcosine (1.0 g, 11.2 mmol) was reacted with chlorotrimethylsilane (2.8 mL, 22.4 mmol) in anhydrous chloroform (25 mL) in the presence of DIEA (4.1 mL, 22.4 mmol). Subsequent reaction of the intermediate with 1-chloro-2-methylpropyl chloroformate (4.59 g, 22.4 mmol) followed by a mixture of DIEA (4.1 mL, 22.4 mmol) and benzoic acid (2.8 g, 22.4 mmol) provided 0.622 g (16.3% yield) of the title compound (50) as a buff-colored solid after aqueous work-up and mass-guided preparative HPLC purification. 1H NMR (CD3OD, 400 MHz): δ=8.13 (d, 2H), 7.81 (d, 1H), 7.61 (m, 3H), 7.57 (m, 5H), 4.10 (br m, 2H), 3.01 (2s, 3H). MS (ESI) m/z 366.14 (M+Na)+.
Sources & evidence
- ORD record
- ord-57302a04ef684888a10dd9997cbec1e0
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07799829B2
Reaction notes
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