تفاعل #534142

ord-e00ce9d0e088452eb1453cc269e1365c

معادلة التفاعل

CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
C[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C
Boc-N(Me)Ala-OH
COC(=O)C1CN(C(=O)OCc2ccccc2)C2CCN(C(=O)C(N)C3CCCCC3)C12
17
COC(=O)C1CN(C(=O)OCc2ccccc2)C2CCN(C(=O)C(N)C3CCCCC3)C12
4-(2-Amino-2-cyclohexyl-acetyl)-hexahydro-pyrrolo[3,2-b]pyrrole-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester
CCN(C(C)C)C(C)C
DIPEA
COC(=O)C1CN(C(=O)OCc2ccccc2)C2CCN(C(=O)C(NC(=O)C(C)N(C)C(=O)OC(C)(C)C)C3CCCCC3)C12
18
المردود 115.7%
COC(=O)C1CN(C(=O)OCc2ccccc2)C2CCN(C(=O)C(NC(=O)C(C)N(C)C(=O)OC(C)(C)C)C3CCCCC3)C12
4-{2-[2-(tert-Butoxycarbonyl-methyl-amino)-propionylamino]-2-cyclohexyl-acetyl}-hexahydro-pyrrolo[3,2-b]pyrrole-1,3-dicarboxylic acid 1-benzyl ester 3-methyl ester
المردود 115.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed successively with 1M HCl, saturated NaHCO3
  2. 2
    تجفيفdried over anhydrous Na2SO4
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated

الإجراء التجريبي

A solution of Boc-N(Me)Ala-OH (113 mg, 0.56 mmol) in NMP (4 mL) was cooled to 0° C. and treated with HATU (207 mg, 0.54 mmol) followed by DIPEA (0.15 mL, 0.87 mmol). After 10 min, 17 (245 mg, 0.55 mmol) in NMP (5 mL) was added. The reaction mixture was allowed to warm to ambient temperature overnight. The solution was diluted with EtOAc, washed successively with 1M HCl, saturated NaHCO3, dried over anhydrous Na2SO4, filtered and concentrated to afford 18 as an orange-colored oil (400 mg) which was used without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08481495B2uspto-grants-2013_07