111210-69-6

Basic information

• Product Name: O-methyl-N-phthaloyl-(S)-tyrosyl chloride
• Synonyms: O-methyl-N-phthaloyl-(S)-tyrosyl chloride
• CAS NO: 111210-69-6
• Molecular Weight: 343.766
• Mol File: 111210-69-6.mol

Chemical Properties

• CAS DataBase Reference: O-methyl-N-phthaloyl-(S)-tyrosyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: O-methyl-N-phthaloyl-(S)-tyrosyl chloride(111210-69-6)
• EPA Substance Registry System: O-methyl-N-phthaloyl-(S)-tyrosyl chloride(111210-69-6)

Safety Data

• Hazardous Substances Data: 111210-69-6(Hazardous Substances Data)

Upstream product

• 52913-16-3 2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(4-methoxyphenyl)-propionic acid 
• 22509-74-6 N-ethoxycarbonylphthalimide 
• 6230-11-1 O-Methyltyrosine 
• 85-44-9 phthalic anhydride 

Downstream Products

• 102314-04-5 4-(O-methyl-N,N-phthaloyl-L-tyrosyl)-morpholine 
• 123885-11-0 O-methyl-N,N-phthaloyl-L-tyrosine-cyclohexylamide 
• 112991-25-0 O-methyl-N,N-phthaloyl-L-tyrosine-(2-hydroxy-ethylamide) 
• 115984-96-8 O-methyl-N,N-phthaloyl-L-tyrosin-anilide 
• 119078-81-8 O-methyl-N,N-phthaloyl-L-tyrosine-benzylamide 
• 51482-37-2 N-[(S)-1-formyl-2-(4-methoxy-phenyl)-ethyl]-phthalimide 
• 56876-12-1 (S)-2-(1,3-dioxoisoindolin-2-yl)-3-(4-methoxyphenyl)propanamide 
• 53-79-2 puromycin 
• 1290176-66-7 (2S)-2-methyl-1-[o-methyl-N-phthaloyl-(S)-tyrosyl]-1,2,3,4-tetrahydroquinoline 
• 200125-70-8 (S)-2-methyl-1,2,3,4-tetrahydroquinoline 
• 1780-19-4 (R)-1,2,3,4-tetrahydroquinaldine 
• 1290176-67-8 (3S)-2,3-dihydro-3-methyl-4-[o-methyl-N-phthaloyl-(S)-tyrosyl]-4H-1,4-benzoxazine 

Relevant articles and documents

Substituent effect on the stereoselectivity of acylation of racemic heterocyclic amines with N-phthaloyl-3-aryl-(S)-alanyl chlorides

The acylative kinetic resolution of racemic 2-methyl-1,2,3,4- tetrahydroquinoline and 2,3-dihydro-3-methyl-4H-1,4-benzoxazine using acyl chlorides of N-phthaloyl-(S)-phenylalanine, N-phthaloyl-3-(4-nitrophenyl)-(S)- alanine and N-phthaloyl-O-methyl-(S)-tyrosine as chiral resolving agents has been carried out. It is shown that the effectiveness of an acylative kinetic resolution depends on the electronic effects of substituents in the phenyl fragment of the acylating agent and increases as the electron-donating properties of the para-substituent (OMe > H > NO2) in phenyl fragment of N-phthaloyl-3-aryl-(S)-alanyl chlorides increase; conducting the process at a reduced temperature also contributes to an enhancement of the kinetic resolution.

Functional primary amines and diamines from α-aminoacids. A concise route to substituted 2-aminotetralins

Image Persented S-Phthalimidomethyl xanthates derived from various r-amino acids add efficiently to a range of unactivated alkenes to give a variety of highly functionalized, protected amines. In the case of phenylalanine and tyrosine derived xanthates, the adducts can be further converted into the rare 4-substituted 2-aminotetralines by a radical ring closure onto the aromatic ring.

Intramolecular Friedel-Crafts Acylation of N-Phthaloyl-Substituted Arylalanyl and Homophenylalanyl Chlorides

N-Phthaloyl-protected arylalanyl and homophenylalanyl chlorides 5 are acylated intramolecularly to 2-phthalimido-1-indanones 6 and -1-tetralone (6d) with AlCl3 (two-fold molar amounts) or catalytic amounts of FeCl3.The cycloacylation to the tetralone 6d with AlCl3 or FeCl3 proceeds without racemisation in very good yields, whereas the cycloacylation to the indanone 6a with FeCl3 gives rise to racemisation.Mixed anhydrides 11 of N-phthaloyl-α-amino acids and trifluoromethanesulfonate were prepared from the N-phthaloylamino acid chlorides and silver triflate.Acylation of arenes 12 with 11a as well as cycloaddition of (S)-O-methyl-N-phthaloyltyrosine triflate can be achieved without racemisation and without a catalyst.