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Hydrochloride methanol → Hydrochloric Acid

HRID 1436021
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인쇄 미리보기

반응식

HRID 1436021 반응식
C(OC([NH:8][CH:9]1[CH2:13][CH2:12][N:11]([S:14]([C:17]2[C:18]3[C:19]([Br:27])=[CH:20][N:21]=[CH:22][C:23]=3[CH:24]=[CH:25][CH:26]=2)(=[O:16])=[O:15])[CH2:10]1)=O)(C)(C)C.[ClH:28].CO>>[NH2:8][CH:9]1[CH2:13][CH2:12][N:11]([S:14]([C:17]2[C:18]3[C:19]([Br:27])=[CH:20][N:21]=[CH:22][C:23]=3[CH:24]=[CH:25][CH:26]=2)(=[O:16])=[O:15])[CH2:10]1.[ClH:28]
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참가 물질

4

반응물 2

HCID 21893726Hydrochloride methanolHCID 67242856(r/s)-3-(Tert-butoxycarbonylamino)-1-(4-bromo-5-isoquinolinesulfonyl)pyrrolidine

생성물 2

HCID 313Hydrochloric AcidHCID 672429043-Amino-1-(4-bromo-5-isoquinolinesulfonyl)pyrrolidine

실험 절차

Intermediate 1 (120 mg) prepared in Step A mentioned above is added with 10% hydrogen chloride/methanol (2 ml, Tokyo Kasei Kogyo), and the mixture is stirred at room temperature for 12 hours. The solvent is concentrated under reduced pressure, and the obtained solid is collected by filtration to obtain the title compound as hydrochloride (84 mg (predictive yield)).

후처리

  1. concentrationThe solvent is concentrated under reduced pressure
  2. filtrationthe obtained solid is collected by filtration

출처 및 근거

ORD 기록
ord-85bfaa3056bf4e0b80ac403742084e55
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07618984B2

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