Trifluoroacetic acid → HCID 123473925, compound

N-tert-butoxycarbonyl-O-propargyl L-seryl glycine methyl ester (6.17 g, 19.6 mmol) was treated with a 50% (v/v) solution of TFA in CH2Cl2 (50 mL). The reaction mixture was stirred for 1 h 20 min before the solvent and bulk of excess TFA was evaporated. The residue was dissolved in H2O (50 mL) and the solution washed with Et2O (3×25 mL). The pH was regulated to pH 10-11 and the solution extracted with CH2Cl2 (3×100 mL). The combined organic extracts were dried with anhydrous MgSO4 and the solvent evaporated affording a yellowish liquid (2.75 g, 65%); δH (300 MHz; d6-DMSO) 8.33 (1H, t/dd, J difficult to measure, NH), 4.14 (2H, d, J 2, CH2CCH), 3.87 (1H, s, CαHH(Gly)), 3.85 (1H, s, CαHH(Gly)), 3.63 (3H, s, OCH3), 3.58 (1H, dd, J 9 and 5, CHH), 3.49 (1H, dd, J 9 and 6, CHH), 3.41 (1H, dd, J 6 and 5, CαH(propSer)), 3.30 (1H, t, J 2, CCH), 1.86 (2H, br s, NH2); δC (75 MHz; d6-DMSO) 173.1, 170.2, 80.1, 77.1, 72.1, 57.6, 54.8, 54.3, 51.6, 40.5

1. customwas evaporated
2. dissolutionThe residue was dissolved in H2O (50 mL)
3. washthe solution washed with Et2O (3×25 mL)
4. extractionthe solution extracted with CH2Cl2 (3×100 mL)
5. dry with materialThe combined organic extracts were dried with anhydrous MgSO4
6. customthe solvent evaporated

ORD record

ord-9fc955b37b3b40a19fb904e2cd1b30eb

Source dataset

uspto-grants-2016_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09227995B2