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Triphenylphosphine → HCID 86661748, 화합물

HRID 879973
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HRID 879973 반응식
[CH2:1]([O:8][C:9]([NH:11][C@@H:12]([CH2:15][NH:16][S:17]([C:20]1[CH:25]=[CH:24][C:23]([O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[CH:22][CH:21]=1)(=[O:19])=[O:18])[CH2:13]O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[NH:52]=[N+:53]=[N-:54].CCOC(/N=N/C(OCC)=O)=O>C1(C)C=CC=CC=1>[CH2:1]([O:8][C:9]([NH:11][C@@H:12]([CH2:15][NH:16][S:17]([C:20]1[CH:21]=[CH:22][C:23]([O:26][C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)=[CH:24][CH:25]=1)(=[O:19])=[O:18])[CH2:13][N:52]=[N+:53]=[N-:54])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 11776TriphenylphosphineHCID 24530Hydrazoic acidHCID 5462977Diethyl azodicarboxylateHCID 66727702HCID 66727702, 화합물

생성물 1

HCID 86661748HCID 86661748, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of (S)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzene sulfonamido) propanol (0.45 g, 1.0 mmol) in toluene (10 mL) was added PPh3 (0.28 g, 1.1 mmol) and the mixture was stirred at RT for 5 min. After adding hydrazoic acid (1.25 M in toluene, 1.04 mL, 1.3 mmol), DEAD (0.17 mL, 1.1 mmol) was added dropwise. The reaction mixture was stirred at RT for 30 min, filtered and solvent was evaporated. The crude residue was chromatographed (silica gel, 30% EtOAc in n-hexane) to afford (R)-2-(benzyloxycarbonylamino)-3-(4-phenoxybenzenesulfon amido) propyl azide as white solid in 60% (0.29 g) yield.

후처리

  1. additionwas added dropwise
  2. stirringThe reaction mixture was stirred at RT for 30 min
  3. filtrationfiltered
  4. customsolvent was evaporated
  5. customThe crude residue was chromatographed (silica gel, 30% EtOAc in n-hexane)

출처 및 근거

ORD 기록
ord-4331b7d309ac4803b1f7197cc9516b7f
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993544B2

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