Benzoic Acid → HCID 24798586, compound

HRID 1715490Notes

Reaction equation

HRID 1715490 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

Loading…