4-Methylmorpholine → HCID 178434957, compound

HRID 448607Notes

Reaction equation

HRID 448607 reaction equation
[C:1]1([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:6]=[CH:5][C:4]([CH2:7][C@@H:8]([NH:17][C:18]([C:20]2[NH:21][N:22]=[N:23][CH:24]=2)=[O:19])[CH2:9][C@:10]([CH2:15][OH:16])([CH3:14])[C:11]([OH:13])=[O:12])=[CH:3][CH:2]=1.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.O[CH2:53][C:54]1[O:55][C:56](=[O:60])[O:57][C:58]=1[CH3:59].CN1CCOCC1>C(Cl)Cl.CC(O)=O>[CH3:59][C:58]1[O:57][C:56](=[O:60])[O:55][C:54]=1[CH2:53][O:12][C:11](=[O:13])[C@@:10]([CH2:15][OH:16])([CH3:14])[CH2:9][C@H:8]([NH:17][C:18]([C:20]1[NH:21][N:22]=[N:23][CH:24]=1)=[O:19])[CH2:7][C:4]1[CH:5]=[CH:6][C:1]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:2][CH:3]=1

Participants

8

Procedure

(2S,4R)-5-Biphenyl-4-yl-2-hydroxymethyl-2-methyl-4-[(3H-[1,2,3]triazole-4-carbonyl)-amino]-pentanoic acid (100 mg, 245 μmol, 1.0 eq.), EDCI (52 μL, 294 μmol, 1.2 eq.) and HOBt (39.7 mg, 294 μmol, 1.2 eq.) were dissolved in DCM (5 mL). After stirring for 10 minutes, 4-hydroxymethyl-5-methyl-[1,3]dioxol-2-one (127 mg, 979 μmol, 4.0 eq.) was added. The mixture was stirred for 1 hour and 4-methylmorpholine (40.4 μL, 1.5 eq.) was added. After 1 hour, the crude material was dissolved in AcOH and purified by preparative HPLC to yield the title compound (20 mg). MS m/z [M+H]+ calc'd for C27H28N4O7, 521.20. found 521.4.

Workup

  1. stirringThe mixture was stirred for 1 hour
  2. waitAfter 1 hour
  3. custompurified by preparative HPLC

Sources & evidence

ORD record
ord-896aefd5097c45d4800ebc24d924f933
Source dataset
uspto-grants-2013_07
Patent number
US08481044B2

Reaction notes

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