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Diisopropylethylamine → 4-(Phenylmethyl) hydrogen L-aspartate

HRID 265230
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HRID 265230 반응식
C1(CCC(N(C)[C@H](C(N[C@H](C(N[C@H](C([NH:34][C@H:35]([C:47]([OH:49])=[O:48])[CH2:36][C:37](=[O:46])[O:38][CH2:39][C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)=O)CC(=O)N)=O)[C@H](CC)C)=O)C(C)C)=O)C=CC=CC=1.N(C(OC(C)(C)C)=O)[C@H](C(O)=O)CC(=O)OCC1C=CC=CC=1.C1C=CC2N(O)N=NC=2C=1.C1CCC(N=C=NC2CCCCC2)CC1.N(C(OC(C)(C)C)=O)[C@H](C(O)=O)CC(=O)N.CC(C)C[C@H](N)C1NN=NN=1.CCN(C(C)C)C(C)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1>CN(C=O)C>[NH2:34][C@H:35]([C:47]([OH:49])=[O:48])[CH2:36][C:37](=[O:46])[O:38][CH2:39][C:40]1[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 7

HCID 81531DiisopropylethylamineHCID 82035N2-((tert-Butoxy)carbonyl)-L-asparagineHCID 199401P,P-Diphenylphosphinic azideHCID 1581888N-tert-Butoxycarbonyl-L-aspartic acid beta-benzyl esterHCID 21712060DCCI HOBtHCID 131720093PhCH2CH2CO-N-Me-Val-Ile-Asn-Asp(OBzl)-OH
HCID 178445939
HCID 178445939, 화합물

생성물 1

HCID 1011864-(Phenylmethyl) hydrogen L-aspartate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A modified procedure of example I was used to assemble the protected tetrapeptide (SEQ ID NO:5) PhCH2CH2CO-N-Me-Val-Ile-Asn-Asp(OBzl)-OH wherein Boc-Asp(OBzl)-OH was linked to the photo-resin and HOBt/DCC was used for coupling Boc-Asn-OH. A solution of the protected tetrapeptide (375 mg, 0.54 mmol) and 3-methyl-1(S)-(5-1H-tetrazolyl)butylamine (375 mg, 1.25 mmol) in DMF (15 ml) was cooled to 0. DIPEA (284 mg) and then diphenylphosphoryl azide (760 mg) were added to the solution. The reaction mixture was stirred for 16 h at 0 and then partitioned between Et2O and H2O containing of few drops of concentrated NH4OH (pH=9.5). The aqueous phase was separated, washed with fresh Et2O and filtered through a 45 m membrane. The pH of the filtrate was adjusted to pH 6.5 by the addition of AcOH and again filtered through a 45 m membrane. The filtrate was loaded on a HPLC preparatory column. The column was eluted with a continuous gradient of 0.06% aqueous TFA in acetonitrile. The pure fractions as indicated by analytical HPLC were combined and lyophilized to give the corresponding Asp(OBzl) protected peptide (132 mg) of the title compound.

후처리

  1. custompartitioned between Et2O and H2O
  2. additioncontaining of few drops of concentrated NH4OH (pH=9.5)
  3. customThe aqueous phase was separated
  4. washwashed with fresh Et2O
  5. filtrationfiltered through a 45 m membrane
  6. additionThe pH of the filtrate was adjusted to pH 6.5 by the addition of AcOH
  7. filtrationagain filtered through a 45 m membrane
  8. washThe column was eluted with a continuous gradient of 0.06% aqueous TFA in acetonitrile

출처 및 근거

ORD 기록
ord-4f09e8f9afa64e4aaf4f7659cdf77203
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05648337

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