L-Alanine → N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanine

HRID 26327

반응식

HRID 26327 반응식
[NH2:1][C@H:2]([C:4]([OH:6])=[O:5])[CH3:3].[NH:7]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[C@H:8]([C:10](ON1C(=O)CCC1=O)=[O:11])[CH3:9].CN1CCOCC1>CN(C=O)C>[NH:7]([C:20]([O:22][C:23]([CH3:24])([CH3:26])[CH3:25])=[O:21])[C@H:8]([C:10]([NH:1][C@H:2]([C:4]([OH:6])=[O:5])[CH3:3])=[O:11])[CH3:9]

참가 물질

5

반응물 3

HCID 5950L-AlanineHCID 79724-MethylmorpholineHCID 11011585Boc-Ala-OSu

생성물 1

HCID 6992569N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

L-Alanine (3.57 g, 40 mmol) was dissolved in 18.8 ml of Triton B (40 mmol), evaporated to dryness, and the oily residue re-evaporated twice with DMF (30 ml each). The salt obtained was stirred with 11.45 g of Boc-Ala-OSu (40 mmol) in 40 ml DMF, with 4 ml of NMM added, for 20 hours. The solvent was removed and the residue taken up in 10% HOAc (100 ml). The product was extracted into EtOAc (4 times 100 ml), washed twice with a small volume of H2O, dried over Na2SO4, evaporated to a small volume, and treated with petroleum ether until cloudiness developed. A crystalline product formed on storage in the refrigerator overnight: Yield, 8.2 g (76.3%); mp 115°-118°.

후처리

  1. customevaporated to dryness
  2. customthe oily residue re-evaporated twice with DMF (30 ml each)
  3. customThe salt obtained
  4. additionadded, for 20 hours
  5. customThe solvent was removed
  6. extractionThe product was extracted into EtOAc (4 times 100 ml)
  7. washwashed twice with a small volume of H2O
  8. dry with materialdried over Na2SO4
  9. customevaporated to a small volume
  10. additiontreated with petroleum ether until cloudiness
  11. customA crystalline product formed on storage in the refrigerator overnight
  12. customYield

출처 및 근거

ORD 기록
ord-9889250ba2dc449bb2d7d2a9635c9889
출처 데이터셋
uspto-grants-1979_04
특허 번호
US04148788

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