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Hydrochloric Acid → KRG-3332 monohydrochloride

HRID 382474
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HRID 382474 반응식
[C:1]([O:7][CH2:8][CH2:9][CH2:10][N:11]1[C:19]2[C:14](=[CH:15][C:16]([CH2:23][C@H:24]([NH:26][CH2:27][CH2:28][O:29][C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=3[O:36][CH2:37][CH3:38])[CH3:25])=[CH:17][C:18]=2[C:20](=[O:22])[NH2:21])[CH:13]=[CH:12]1)(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3].[ClH:39]>C(O)C>[ClH:39].[C:1]([O:7][CH2:8][CH2:9][CH2:10][N:11]1[C:19]2[C:14](=[CH:15][C:16]([CH2:23][C@H:24]([NH:26][CH2:27][CH2:28][O:29][C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][C:31]=3[O:36][CH2:37][CH3:38])[CH3:25])=[CH:17][C:18]=2[C:20](=[O:22])[NH2:21])[CH:13]=[CH:12]1)(=[O:6])[C:2]([CH3:4])([CH3:5])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 9872508KRG-3332 free base

생성물 1

HCID 9872507KRG-3332 monohydrochloride

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of (R)-3-[7-carbamoyl-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-1H-indol-1-yl]propyl pivalate (6.07 g) in ethanol (58 ml) was added dropwise 1N hydrochloric acid (11.6 ml) under ice-cooling with stirring, and the mixture was stirred for 15 minutes under the same condition. The reaction mixture was concentrated in vacua, and to the residue was added ethanol. After azeotropic removal of water, the residue was dissolved in ethanol (6 ml) and ethyl acetate (60 ml) was added to the solution. After the mixture was allowed to stand for 16 hours at room temperature, the resulting colorless crude crystals (5.14 g) were obtained. After the crystals were combined with another crude crystals obtained similarly, recrystallization of the combined crystal (8.12 g) from ethanol/ethyl acetate (15/1) gave (R)-3-[7-carbamoyl-5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-1H-indol-1-yl]propyl pivalate hydrochloride (7.46 g) as colorless crystals.

후처리

  1. temperaturecooling
  2. stirringthe mixture was stirred for 15 minutes under the same condition
  3. concentrationThe reaction mixture was concentrated in vacua
  4. additionto the residue was added ethanol
  5. customAfter azeotropic removal of water
  6. dissolutionthe residue was dissolved in ethanol (6 ml)
  7. additionethyl acetate (60 ml) was added to the solution
  8. customthe resulting colorless crude crystals (5.14 g) were obtained
  9. customobtained similarly
  10. customrecrystallization of the combined crystal (8.12 g) from ethanol/ethyl acetate (15/1)

출처 및 근거

ORD 기록
ord-f1a697a8eb5f4c3f9fd73189fabc4496
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06310086B1

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