تفاعل #1813

ord-bcef87ed7a7043ef86ee001ff10769ae

معادلة التفاعل

CC(C)(C)OC(=O)NCC(=O)O
Boc-Gly
CCN=C=NCCCN(C)C
N-ethyl-N'(dimethylaminopropyl)carbodiimide
Cc1ccc(CO[C@H]2[C@H](O)[C@H](O)C(O)O[C@@H]2CO)cc1.N[C@@H](CC(=O)OC1CCCCC1)C(=O)O
Asp(O-cHex) Man(4-MBzl)
CN(C)C=O
DMF
On1nnc2ccccc21
N-Hydroxybezotriazole
CC(C)(C)OC(=O)NCC(=O)N[C@@H](CC(=O)OC1CCCCC1)C(=O)O.Cc1ccc(CO[C@H]2[C@H](O)[C@H](O)C(O)O[C@@H]2CO)cc1
titled compound
المردود 89.2%
CC(C)(C)OC(=O)NCC(=O)N[C@@H](CC(=O)OC1CCCCC1)C(=O)O.Cc1ccc(CO[C@H]2[C@H](O)[C@H](O)C(O)O[C@@H]2CO)cc1
Boc-Gly-Asp(O-cHex) Man(4-MBzl)
المردود 89.2%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred for 18 h
  2. 2
    تركيزThe reaction mixture was concentrated to a small volume
  3. 3
    workup.ADDITIONpoured into 1.5 L of aqueous 10% K2CO3
  4. 4
    ترشيحThe precipitated product was collected by filtration
  5. 5
    غسيلwas washed with water to a neutral pH

الإجراء التجريبي

To a cold solution of Asp(O-cHex)-Man(4-MBzl) (46.7 g, 86.4 mmol) in DMF (100 mL) diisopropylethylamine (15 mL, 86.1 mmol) was added. N-Hydroxybezotriazole (14.0 g, 104 mmol) was added followed by Boc-Gly (16.6 g, 94.8 mmol). The reaction mixture was stirred in the cold for a few minutes, and N-ethyl-N'(dimethylaminopropyl)carbodiimide (18.2 g, 94.9 mmol) was added. The reaction mixture was allowed to warm to room temperature and stirred for 18 h. The reaction mixture was concentrated to a small volume and poured into 1.5 L of aqueous 10% K2CO3. The precipitated product was collected by filtration and was washed with water to a neutral pH to afford the titled compound (50.6 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726192uspto-grants-1998_03