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Hydrochloric Acid → 4,5-Dihydro-4[5-(amino)pentan-1-yl]-3h-1,4,8b-triazaacenaphthylen-5-one.dihydrochloride

HRID 1068725
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인쇄 미리보기

반응식

HRID 1068725 반응식
C(OC([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:14]1[C:24](=[O:25])[C:23]2[N:26]3[C:16](=[CH:17][N:18]=[C:19]3[CH:20]=[CH:21][CH:22]=2)[CH2:15]1)=O)(C)(C)C.[ClH:27]>C(O)C>[ClH:27].[ClH:27].[NH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][N:14]1[C:24](=[O:25])[C:23]2[N:26]3[C:16](=[CH:17][N:18]=[C:19]3[CH:20]=[CH:21][CH:22]=2)[CH2:15]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 211901734,5-Dihydro-4[5-(tert-butoxycarbonylamino)pentan-1-yl]-3H-1,4,8b-triazaacenaphthylen-5-one

생성물 1

HCID 218465014,5-Dihydro-4[5-(amino)pentan-1-yl]-3h-1,4,8b-triazaacenaphthylen-5-one.dihydrochloride

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 2.24 g (6.25 mmol) of 4,5-dihydro-4[5-(tert-butoxycarbonylamino)pentan-1-yl]-3H-1,4,8b-triazaacenaphthylen-5-one in 20 ml of ethanol was added 20 ml of conc. HCl. The mixture was stirred for 1.5 hour at room temperature. The solvent was distilled off to leave 2.05 g of the desired compound (quant. a pale brown solid). This product was used in the subsequent reaction without further purification.

후처리

  1. distillationThe solvent was distilled off

출처 및 근거

ORD 기록
ord-94b7f1198d414a29933569e98e947b9a
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06251905B1

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