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Hydrochloric Acid → HCID 67555450, 화합물

HRID 1419588
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HRID 1419588 반응식
[ClH:1].C(OC([N:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[CH2:21][NH:22][S:23]([CH3:26])(=[O:25])=[O:24])[CH2:11][CH2:10]1)=O)(C)(C)C>CO>[ClH:1].[N:12]1([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[CH2:21][NH:22][S:23]([CH3:26])(=[O:25])=[O:24])[CH2:13][CH2:14][NH:9][CH2:10][CH2:11]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 542677021-Boc-4-[2-(methanesulfonylamino-methyl)-phenyl]-piperazine

생성물 1

HCID 67555450HCID 67555450, 화합물수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Methanolic hydrogen chloride (4M, 2.5 mL) was added to a stirred, cooled (0° C.) suspension of N-[2-(4-t-butoxycarbonylpiperazin-1-yl)phenylmethyl]methanesulfonamide (330 mg, 0.89 mmol) in methanol (1 mL) and the mixture was stirred at room temperature for 4 h. The solvent was evaporated under reduced pressure to give the title compound as an off-white solid (269 mg, 99%), δH (360 MHz, d6 -DMSO) 9.15 (2H, br s), 7.44 (1H, d, J 7.6 Hz), 7.42 (1H, br t, J 5.6 Hz), 7.31 (1H, t, J 7.6 Hz), 7.16 (2H, m), 4.22 (2H, d, J 5.6 Hz), 3.23 (4H, m), 3.06 (4H, m), and 2.92 (3H, s). m/e (ES+) 270 (MH+).

후처리

  1. temperaturecooled
  2. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-76601a9d2b994f18a6885fb4ff00f69a
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05885999

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