Dimethylformamide → HCID 19800031, 화합물

HRID 1646871노트

반응식

HRID 1646871 반응식
Br[C:2]1[CH:3]=[N:4][C:5]2[C:10]([C:11]=1[NH:12][CH2:13][C:14]1([OH:20])[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)=[CH:9][CH:8]=[CH:7][CH:6]=2.CC(C)([O-])C.[K+].CN(C=O)C>O>[N:12]1[C:11]2[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[N:4]=[CH:3][C:2]=2[O:20][C:14]2([CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH:13]=1

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 14209243HCID 14209243, 화합물HCID 23665647Potassium tert-butoxide

생성물 1

HCID 19800031HCID 19800031, 화합물

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
130 °C

실험 절차

A mixture of 5.5 g of 3-bromo-N-(1-hydroxycyclohexylmethyl)-4-quinolinamine, 2.2 g of potassium tert-butoxide and 50 ml of DMF was heated at 130° C. for 1 hour and then poured into 250 ml of water. The product was extracted with dichloromethane and ethyl acetate, dried and concentrated, and the residue was purifed by HPLC using dichloromethane:MeOH=95:5 as the eluent. The fractions containing the product were combined and concentrated. The residue was taken up in water and stirred for 1 hour, and the solid was filtered and recrystallized from toluene. The yield was 2.6 g, mp 164°-165° C.

후처리

  1. extractionThe product was extracted with dichloromethane and ethyl acetate
  2. customdried
  3. concentrationconcentrated
  4. additionThe fractions containing the product
  5. concentrationconcentrated
  6. filtrationthe solid was filtered
  7. customrecrystallized from toluene

출처 및 근거

ORD 기록
ord-9e7f6e2fb44e4ca8aa676b47b60a3cfc
출처 데이터셋
uspto-grants-1993_01
특허 번호
US05182275

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