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4-Methylmorpholine → carbobenzoxy-beta-alanyl-L-proline t-butyl ester

HRID 27347
노트
인쇄 미리보기

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HRID 27347 반응식
[C:1]([NH:11][CH2:12][CH2:13][C:14]([OH:16])=O)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].CN1CCOCC1.C(OC(Cl)=O)C(C)C.Cl.[C:33]([O:37][C:38](=[O:44])[C@@H:39]1[CH2:43][CH2:42][CH2:41][NH:40]1)([CH3:36])([CH3:35])[CH3:34]>C(N(CC)CC)C.CN(C)C=O.O1CCCC1>[C:33]([O:37][C:38](=[O:44])[C@@H:39]1[CH2:43][CH2:42][CH2:41][N:40]1[C:14](=[O:16])[CH2:13][CH2:12][NH:11][C:1]([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2])([CH3:36])([CH3:34])[CH3:35]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 79724-MethylmorpholineHCID 62365Isobutyl chloroformateHCID 75313N-Benzyloxycarbonyl-beta-alanineHCID 6453107tert-Butyl L-prolinate hydrochloride

생성물 1

HCID 54135485carbobenzoxy-beta-alanyl-L-proline t-butyl ester

시약·촉매·용매 3

HCID 6228Dimethylformamide
용매
HCID 8028Tetrahydrofuran용매
HCID 8471Triethylamine용매

실험 절차

4.46 g. of carbobenzoxy-β-alanine is dissolved in 20 ml. of tetrahydrofuran and the resulting solution cooled to -10° C. With constant stirring of the solution, 2.4 ml. of N-methylmorpholine followed by 2.6 ml. of isobutylchloroformate are added and the resulting reaction mixture is stirred thereafter for approximately 5 minutes at -10° C. 4.16 g. of L-proline t-butyl ester hydrochloride in 20 ml. of dimethylformamide and 2.8 ml. of triethylamine is added to the reaction mixture which is thereafter stirred overnight, while slowly warming to room temperature. The solvent of the reaction mixture is evaporated in vacuo at 30°-35°. The residue is dissolved in 800 ml. of ethyl acetate which is washed with (2×150 ml.) a 10% citric acid solution, with (1×150 ml.) water, with (2×150 ml.) saturated solution of sodium bicarbonate and then with (2×100 ml.) water. The organic layer is dried with anhydrous magnesium sulfate and the solvent evaporated to yield carbobenzoxy-β-alanyl-L-proline t-butyl ester.

후처리

  1. customthe resulting reaction mixture
  2. stirringis stirred
  3. stirringis thereafter stirred overnight
  4. customThe solvent of the reaction mixture is evaporated in vacuo at 30°-35°
  5. dissolutionThe residue is dissolved in 800 ml
  6. washof ethyl acetate which is washed with (2×150 ml.) a 10% citric acid solution
  7. dry with materialThe organic layer is dried with anhydrous magnesium sulfate
  8. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-c7cd6af73aca49feafad7a587907044d
출처 데이터셋
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04221706

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