تفاعل #415375

ord-f804dd27906d42eeb423a044dbb2edbc

معادلة التفاعل

NCCC[C@H](N)C(=O)O
Orn
N=C(N)NCCC[C@H](N)C(=O)O
Arg
N=C(N)NCCC[C@H](N)C(=O)O
Arg
Br
hydrogen bromide
C[C@@H](O)[C@H](N)C(=O)O
Thr
NCCCC[C@H](N)C(=O)O
Lys
N=C(N)NCCC[C@H](N)C(=O)O
Arg

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat room temperature
  2. 2
    أخرىfor 1- 1/2 hours
  3. 3
    أخرىIt is then dried in vacuo
  4. 4
    غسيلwashed twice with water
  5. 5
    أخرىthe peak of absorption

الإجراء التجريبي

30 mg. of the tetrapeptide resin are hydrolyzed with 6 N hydrochloric acid in dioxane for 18 hours and the product assayed on the amino acid analyzer. It yields a ratio of Thr 1, Lys 1, Pro 1, Arg 1. The value for Arg is the sum of Arg, Orn and nitro Arg. The tetrapeptide is cleaved off the resin with hydrogen bromide in TFA at room temperature for 1- 1/2 hours. It is then dried in vacuo, washed twice with water and lyophilized. Its weight of 176 mg. represents a 78% yield based on Lys. It is then taken up in 10 ml. of methanol containing 10% acetic acid. This is then exposed to catalytic hydrogenation with twice its weight 350 mg. of palladium on barium sulfate in a hydrogen atmosphere at 60 pounds per square inch pressure with continuous shaking for 24 hours at which time no nitro Arg is detected at 271 mμ, the peak of absorption. An aliquot is again hydrolyzed with 6 N HC1 in water and assayed. This yields a comparable figure for Thr, Lys, Pro, and Arg.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04016259uspto-grants-1977_04