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Phthalimide → HCID 12803194, 화합물

HRID 980289
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HRID 980289 반응식
[N:1](C(OCC)=O)=NC(OCC)=O.[C:13]1([CH2:19][O:20][C:21](=[O:36])[NH:22][CH2:23][CH2:24][C:25]2[C:33]3[C:28](=[CH:29][CH:30]=[C:31]([CH2:34]O)[CH:32]=3)[NH:27][CH:26]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(=O)NC(=O)C2=CC=CC=C12>O1CCCC1>[C:13]1([CH2:19][O:20][C:21](=[O:36])[NH:22][CH2:23][CH2:24][C:25]2[C:33]3[C:28](=[CH:29][CH:30]=[C:31]([CH2:34][NH2:1])[CH:32]=3)[NH:27][CH:26]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6809PhthalimideHCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 20197302HCID 20197302, 화합물

생성물 1

HCID 12803194HCID 12803194, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of diethyl azodicarboxylate (1.48 g) in dry tetrahydrofuran (THF) (8 ml) was added over 2 min., keeping the temperature at 25°, to a stirred solution of phenylmethyl[2-[5-(hydroxymethyl)-1H-indol-3-yl]ethyl]carbamate (2.6 g), triphenylphosphine (2.35 g) and phthalimide (1.75 g) in THF (20 ml). After 4 h, the solvent was evaporated in vacuo and the residue was dissolved in a solution of hydrazine hydrate (15 ml) in ethanol (100 ml).

후처리

  1. customat 25°
  2. customthe solvent was evaporated in vacuo
  3. dissolutionthe residue was dissolved in a solution of hydrazine hydrate (15 ml) in ethanol (100 ml)

출처 및 근거

ORD 기록
ord-a978ec6ad51f486190c241e071ae036b
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04636521

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