Glycerol → HCID 23387485, compound

HRID 1790810Notes

Reaction equation

HRID 1790810 reaction equation
[C:1]([NH:11][C@H:12]([C:16]([OH:18])=[O:17])[CH:13]([CH3:15])[CH3:14])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].[OH:19][CH2:20][CH:21]([CH2:23]O)[OH:22].C1(N=C=NC2CCCCC2)CCCCC1.CCOC(C)=O.CCCCCC>CN(C)C1C=CN=CC=1.C(Cl)Cl.CO>[C:1]([NH:11][C@H:12]([C:16]([O:18][CH2:23][CH:21]([CH2:20][OH:19])[OH:22])=[O:17])[CH:13]([CH3:14])[CH3:15])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2]

Participants

7

Reactant 4

HCID 753GlycerolHCID 10868DicyclohexylcarbodiimideHCID 726987N-Carbobenzoxy-L-valineHCID 21226206Ethyl acetate hexane

Product 1

HCID 23387485HCID 23387485, compound

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 21226129Dichloromethane methanolSolvent

Procedure

CBz-L-valine (4.35 g, 17.3 mmol) was added to a fivefold excess of glycerol (8 ml, 86.9 mmol) togehter with dicyclohexylcarbodiimide (4.29 g 20.8 mmol) and 4-dimethylaminopyridine (0.212 g) at room temperature. After stirring overnight the suspension was filtered and DMF removed in vacuo from the filtrate. The residue was redissolved in CH2Cl2, washed successively with saturated NaHCO3, brine, and water and then dried. The crude material was chromatographed on silica gel with 4/1 EtOAc—hexane as eluent to yield 2.465 g. Rf (4/1 EtOAc—hexane) 0.17, (20/1 CH2Cl2-methanol) 0.12.

Workup

  1. filtrationwas filtered
  2. customDMF removed in vacuo from the filtrate
  3. dissolutionThe residue was redissolved in CH2Cl2
  4. washwashed successively with saturated NaHCO3, brine, and water
  5. customdried
  6. customThe crude material was chromatographed on silica gel with 4/1 EtOAc—hexane as eluent
  7. customto yield 2.465 g

Sources & evidence

ORD record
ord-e586d689a95a4d88aef4134ac987ac55
Source dataset
uspto-grants-2006_07
Patent number
US07071173B2

Reaction notes

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