تفاعل #46049

ord-0538aae722e14b908383f853c6c8fd6d

معادلة التفاعل

CCN(C(C)C)C(C)C
diisopropylethylamine
CS(=O)(=O)Cl
Methanesulfonyl chloride
CCN(C(C)C)C(C)C
diisopropylethylamine
CC(C)(C)OC(=O)N[C@H](C(=O)O)C12CC3CC(CC(O)(C3)C1)C2
(αS)-α[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid
CC(C)(C)OC(=O)N[C@H](C(=O)O)C12CC3CC(CC(O)(C3)C1)C2
Formula 3
CC(C)(C)OC(=O)N[C@H](C(=O)O)C12CC3CC(CC(O)(C3)C1)C2
(αS)-α[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid
Cl.NC(=O)[C@@H]1C[C@@H]2C[C@@H]2N1
(1S,3S,5S)-2-azabicyclo[3.1.0]hexane-3-carboxamide hydrochloride salt
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
CC(C)(C)OC(=O)N[C@H](C(=O)N1[C@H](C#N)C[C@@H]2C[C@@H]21)C12CC3CC(CC(O)(C3)C1)C2
3-cyano-(αS)-α-(3-hydroxytricyclo[3.3.1.13,7]dec-1-yl)-β-oxo-(1S,3S,5S)-2-azabicyclo[3.1.0]hexane-2-ethanecarbamic acid, 1,1-dimethylethyl ester

المذيبات

ظروف التفاعل

درجة الحرارة
-6°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 2 L three-necked flask equipped with a thermometer, a mechanical stirrer and a gas inlet
  2. 2
    أخرىto produce a clear solution
  3. 3
    أخرىthe internal temperature below 8° C
  4. 4
    workup.STIRRINGThe reaction mixture was stirred at 0° C. until all acid
  5. 5
    أخرىthe flask was removed from the cooling bath
  6. 6
    workup.STIRRINGThe reaction mixture was stirred at room temperature for 2 hours

الإجراء التجريبي

A 2 L three-necked flask equipped with a thermometer, a mechanical stirrer and a gas inlet was charged with (αS)-α[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula 3) (50 grams, 153.8 mmol). THF (200 ml) was added and stirred to produce a clear solution. The solution was cooled to −6° C. in an acetone-dry ice-water bath. Methanesulfonyl chloride (Mes-Cl) (13.1 ml, 169 mmol, 1.1 equivalents) was then added as a single portion followed by diisopropylethylamine (94 ml, 539 mmol, 1.1 equivalents). The diisopropylethylamine was added slowly over a period of about 4 minutes to keep the internal temperature below 8° C. The reaction mixture was stirred at 0° C. until all acid was converted to mixed anhydride. (1S,3S,5S)-2-azabicyclo[3.1.0]hexane-3-carboxamide hydrochloride salt (32.5 grams, 200 mmol, 1.1 equivalents) and hydroxybenzotriazole (HOBT) (1.04 grams, 7.6 mmol, 0.05 equivalents) were then added in a single portion and the flask was removed from the cooling bath. The reaction mixture was stirred at room temperature for 2 hours and then left overnight at room temperature.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07741082B2uspto-grants-2010_06