Methanol → 4-[[(Diisopropylamino)methylene]amino]-3-pyridinol N,N-dimethyl carbamate

HRID 361350

반응식

HRID 361350 반응식
[CH:1]([N:4]([CH:8]=[N:9][C:10]1[CH:15]=[CH:14][N:13]=[CH:12][C:11]=1[OH:16])[CH:5]([CH3:7])[CH3:6])([CH3:3])[CH3:2].C(N(CC)CC)C.[CH3:24][N:25]([CH3:29])[C:26](Cl)=[O:27].CO>CCOCC.C(Cl)Cl>[CH3:24][N:25]([CH3:29])[C:26]([O:16][C:11]1[CH:12]=[N:13][CH:14]=[CH:15][C:10]=1[N:9]=[CH:8][N:4]([CH:5]([CH3:7])[CH3:6])[CH:1]([CH3:2])[CH3:3])=[O:27]

참가 물질

7

반응물 4

HCID 887MethanolHCID 6598Dimethylcarbamoyl ChlorideHCID 8471TriethylamineHCID 153809314-[[(Diisopropylamino)methylene]amino]-3-pyridinol

생성물 1

HCID 677490834-[[(Diisopropylamino)methylene]amino]-3-pyridinol N,N-dimethyl carbamate

시약·촉매·용매 2

HCID 3283Diethyl Ether용매2회HCID 6344Dichloromethane용매

실험 절차

To a stirred mixture of 4-[[(diisopropylamino)methylene]amino]-3-pyridinol (1.06 g) and triethylamine (1.0 ml) in 25 ml dry Et2O was added dimethyl carbamyl chloride (0.53 ml). The mixture was stirred at room temperature for 2 hours, after which no starting material remained as seen by TLC (silica, 10:90 CH3OH:CH2Cl2). The mixture was diluted with 25 ml Et2O, filtered, washed with Et2O, and the filtrate concentrated in vacuo and chromatography on silica using EtOAc eluent. The fractions containing desired product were combined and concentrated to provide 500 mg of pure product. Another run was carried out in the same manner as above using 740 mg of starting material. The products from both runs were combined. Recrystallization attempts failed, and the product was dried in vacuo to provide 790 mg of a white solid, m.p. 76°-79° C.

후처리

  1. filtrationfiltered
  2. washwashed with Et2O
  3. concentrationthe filtrate concentrated in vacuo and chromatography on silica
  4. additionThe fractions containing desired product
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ed1b7778d41e49f480131e87578f4714
출처 데이터셋
uspto-grants-1999_02
특허 번호
US05866565

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