HCID 118896811, compound → HCID 118896739, compound

Temperature

0 °C

The peptide (1 g) was then dissolved in trifluoroacetic acid (1.25 ml) and the mixture was stirred at 0° C. for 10 mins and allowed to warm to room temperature and stirred for a further 40 mins. The solvents were removed in vacuo. This was re-dissolved in DCM and washed with cold saturated NaHCO3 (10 ml). The organic layer was dried with Na2SO4 and the solvent removed in vacuo to give the deprotected peptide benzyl4-(3-(1H-indol-3-yl)-1-methoxy-1-oxopropan-2-ylamino)-3-((2S)-2-(2-aminopropanamido)-4-(methylthio)butanamido)-4-oxobutanoate as a dark yellow thick oil. 1H NMR 300 MHz δH(ppm): 1.49 (3H, t), 2.06 (2H, t), 2.20 (3H, s), 2.69(3H, dt), 2.90(1H, dd), 3.08 (1H, q), 3.29 (1H, td), 3.70 (3H, s) 3.75 (1H, q), 4.09 (1H, t), 4.29 (1H, t), 5.02 (1H, d), 5.10 (1H, t), 6.96 (2H, q), 7.15 (5H, sep), 7.30 (7H, m), 7.60 (1H, d), 8.40 (1H, d), 8.51 (1H, s); 13C NMR (75 MHz) δC: 15.18(S—CH3), 27.83(CH2—In), 29.78(CH2—S), 30.22(CH2—CH2S), 37.60(CH2—C═O), 50.74(CH—CH3), 51.15(CH3—COO), 51.45 (CH), 52.07(CH—CH2), 55.52(CH—CH2), 66.87(O—CH2—Bn), 108.99(In), 111.30(In), 118.72(In), 119.52(In), 122.16(In), 123.12(In), 127.02(Bn), 127.12(Bn), 127.47(In), 128.29(Bn), 128.58(Bn), 128.65(Bn), 136.13(Bn), 136.34(Bn), 166.62(C═O), 166.99(C═O), 167.29(C═O), 170.38(C═O), 170.67(C═O) ESI-MS calculated for C31H39N5O7SNa, 648.2470 found M+Na, 648.2482. AlanylMethionylaspartyl(benzyl)tryptophan methyl ester (0.5 g) was then dissolved in ethanol and Pd/C was added. The reaction mixture was then placed in a hydrogenator and shaken overnight. The mixture was filtered through celite and the filtrate was collected. The solvent was removed in vacuo and the residue material was dissolved in dichloromethane (5 ml) and cooled to 0° C. The peptide (0.5 g) was then dissolved in a mixture of methanol (3 ml) and 1M NaOH (3 ml) and stirred at RT for 1 hour. To this water (6 ml) was added and extracted with ether (6 ml). The aqueous phase was acidified to pH 3 with 3M citric acid. The resultant oil was extracted with ethyl acetate (2×10 ml). The combined extracts were dried over Na2SO4 to yield the free acid. 1H NMR (600 MHz) δH: 1.40 (3H, t), 1.87 (2H, m), 1.93 (3H, s), 2.34 (2H, q), 2.41 (1H, dd), 2.56 (1H, dd), 3.13 (1H, dd), 3.26 (1H, dd), 3.98 (1H, q), 4.25 (1H, q), 4.43 (1H, t), 4.49 (1H, q), 7.10 (1H, t), 7.14 (1H, s), 7.17 (3H, t), 7.43 (1H, d), 7.61 (1H, d)13C NMR (150 MHz)δC: 14.08 (S—CH3), 16.36 (—CH3), 29.17 (CH2CH2—S), 29.69 (CH2CH2—S), 38.33 (CH2—CO2H), 27.27 (CH2—In), 48.89 (CH—CH3), 52.62 (CHCH2—In), 51.47 (CHCH2CH2—S), 55.58 (CHCH2CO2H), 111.75 (arom), 118.70 (arom), 119.16 (arom), 121.71 (arom), 124.20 (arom), 127.34 (arom), 135.97 (arom), 147.32 (arom), 170.61 (CONH), 171.81 (CONH), 172.57 (CONH), 177.65 (CO2H), 177.90 (CO2H).

1. filtrationThe mixture was filtered through celite
2. customthe filtrate was collected
3. customThe solvent was removed in vacuo
4. dissolutionthe residue material was dissolved in dichloromethane (5 ml)
5. dissolutionThe peptide (0.5 g) was then dissolved in a mixture of methanol (3 ml) and 1M NaOH (3 ml)
6. stirringstirred at RT for 1 hour
7. additionTo this water (6 ml) was added
8. extractionextracted with ether (6 ml)
9. extractionThe resultant oil was extracted with ethyl acetate (2×10 ml)
10. dry with materialThe combined extracts were dried over Na2SO4
11. customto yield the free acid

ORD record

ord-0ac9d722ff1243e0868f172ae3b44767

Source dataset

uspto-grants-2016_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09399661B2