Triethylamine → 5-chloro-3-(L-gamma-glutamylamino)benzoic acid
Reaction equation
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C1C=NC2N(O)N=NC=2C=1.[NH:35](C(OC(C)(C)C)=O)[C@H:36]([C:42]([O:44]C(C)(C)C)=[O:43])[CH2:37][CH2:38][C:39](=O)[OH:40].Cl.C(N(CC)CC)C.[Cl:64][C:65]1[CH:66]=[C:67]([NH2:75])[CH:68]=[C:69]([CH:74]=1)[C:70]([O:72]C)=[O:71]>ClCCl>[Cl:64][C:65]1[CH:66]=[C:67]([NH:75][C:39](=[O:40])[CH2:38][CH2:37][C@@H:36]([C:42]([OH:44])=[O:43])[NH2:35])[CH:68]=[C:69]([CH:74]=1)[C:70]([OH:72])=[O:71]Participants
7
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
38 mg (0.1 mmol) of HATU, 14 mg (0.1 mmol) of HOAt, 30 mg (0.1 mmol) of Boc-Glu-OtBu hydrochloride, 0.014 mL (0.1 mmol) of triethylamine and 1 mL of dichloromethane were added to 30 mg (0.1 mmol) of methyl 5-chloro-3-aminobenzoate, and stirred at room temperature overnight.
Sources & evidence
- ORD record
- ord-4b507a098ec34025a572dc0bf0d77144
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09174932B2
Reaction notes
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