Sodium hydride → ethyl 6-[4-[N-(4-pyridyl)-N-tertiary-butyloxycarbonylamino]phenoxy]hexanoate

HRID 2238

반응식

HRID 2238 반응식
[H-].[Na+].[N:3]1[CH:8]=[CH:7][C:6]([N:9]([C:17]2[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=2)[C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:5][CH:4]=1.Br[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31]>CN(C=O)C>[N:3]1[CH:8]=[CH:7][C:6]([N:9]([C:17]2[CH:18]=[CH:19][C:20]([O:23][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:21][CH:22]=2)[C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:5][CH:4]=1

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 117544Ethyl 6-bromohexanoateHCID 18918286tert-butyl N-(4-hydroxyphenyl)-N-(pyridin-4-yl)carbamate

생성물 1

HCID 18918347ethyl 6-[4-[N-(4-pyridyl)-N-tertiary-butyloxycarbonylamino]phenoxy]hexanoate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Sodium hydride (50% w/w dispersion in mineral oil, 55 mg) was added under argon to a stirred solution of the product from step (iii) above (300 mg) in dry DMF (5 ml). After five minutes, ethyl 6-bromohexanoate (0.20 ml) was added and the mixture stirred for 16 hours. The DMF was evaporated in vacuo and the residue partitioned between dichloromethane and water. The aqueous phase was extracted with further dichloromethane. The combined organic extracts were washed with water then dried, and evaporated. The residue was purified by chromatography on alumina, eluting with dichloromethane and then 1% v/v methanol/dichloromethane. Evaporation of the appropriate fractions gave ethyl 6-[4-[N-(4-pyridyl)-N-tertiary-butyloxycarbonylamino]phenoxy]hexanoate, 260 mg, as a yellow gum: NMR (CDCl3) δ 8.40 (2H, dd), 7.16 (2H, dd), 7.07 (2H, m), 6.90 (2H, m), 4.13 (2H, q), 3.98 (2H, t), 2.34 (2H, t), 1.78 (4H, m), 1.57 (2H, m), 1.44 (9H, s), 1.26 (3H, t); m/e 429 (M+H)+.

후처리

  1. customThe DMF was evaporated in vacuo
  2. customthe residue partitioned between dichloromethane and water
  3. extractionThe aqueous phase was extracted with further dichloromethane
  4. washThe combined organic extracts were washed with water
  5. customthen dried
  6. customevaporated
  7. customThe residue was purified by chromatography on alumina
  8. washeluting with dichloromethane
  9. customEvaporation of the appropriate fractions

출처 및 근거

ORD 기록
ord-406919881ea245cf8271f8faf8e54070
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05728701

연결된 노트

불러오는 중…