Sodium hydride → 6-(3-Dimethylaminopropyl)-1,9-dimethyl-7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole dihydrochloride

HRID 647947노트

반응식

HRID 647947 반응식
[CH3:1][C:2]1[C:6]2=[C:7]3[C:11](=[CH:12][CH:13]=[C:5]2[S:4][CH:3]=1)[NH:10][C:9]1[CH2:14][CH2:15][N:16]([CH3:18])[CH2:17][C:8]3=1.[H-].[Na+].[CH3:21][N:22]([CH3:27])[CH2:23][CH2:24][CH2:25][Cl:26]>CN(C)C=O>[ClH:26].[ClH:26].[CH3:21][N:22]([CH3:27])[CH2:23][CH2:24][CH2:25][N:10]1[C:11]2[C:7](=[C:6]3[C:2]([CH3:1])=[CH:3][S:4][C:5]3=[CH:13][CH:12]=2)[C:8]2[CH2:17][N:16]([CH3:18])[CH2:15][CH2:14][C:9]1=2

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 669603-Chloro-N,N-dimethyl-1-propanamineHCID 71140Tienocarbine

생성물 1

HCID 204843326-(3-Dimethylaminopropyl)-1,9-dimethyl-7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole dihydrochloride

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4.0 g of 1,9-dimethyl-7,8,9,10-tetrahydrothieno[3,2-e]pyrido[4,3-b]indole are dissolved in 60 ml of dimethylformamide, 0.78 g of a 50% strength dispersion of NaH is added, whilst stirring, and, after 1 hour, 2.4 g of 3-dimethylaminopropyl chloride are added. After leaving the mixture is stand for 15 hours, the solvent is evaporated off, the residue is taken up in ethyl acetate, the ethyl acetate mixture is washed and dried and the product is purified on SiO2 with chloroform/methanol (1:1). The dihydrochloride is then prepared with isopropyl alcohol/HCl. Melting point: 263° C.

후처리

  1. customAfter leaving the mixture
  2. customfor 15 hours
  3. customthe solvent is evaporated off
  4. washthe ethyl acetate mixture is washed
  5. customdried
  6. customthe product is purified on SiO2 with chloroform/methanol (1:1)
  7. customThe dihydrochloride is then prepared with isopropyl alcohol/HCl

출처 및 근거

ORD 기록
ord-955e843a4889417c8d3ad22bb3185a4a
출처 데이터셋
uspto-grants-1983_10
특허 번호
US04410536

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