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Hydrochloric Acid → HCID 67721738, 화합물

HRID 54688
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HRID 54688 반응식
C([N:4]1[CH2:13][C@H:12]([C:14]2[CH:19]=[CH:18][C:17]([O:20]C)=[C:16]([O:22]C)[CH:15]=2)[C:11]2[C:6](=[C:7]([O:26]C)[C:8]([O:24]C)=[CH:9][CH:10]=2)[CH2:5]1)(=[O:3])C.[ClH:28]>C(O)C>[OH2:3].[ClH:28].[OH:24][C:8]1[C:7]([OH:26])=[C:6]2[C:11]([C@@H:12]([C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[C:16]([OH:22])[CH:15]=3)[CH2:13][NH:4][CH2:5]2)=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 54226046(R)-(-)-N-acetyl-7,8-dimethoxy-4-(3,4-dimethoxyphenyl)-1,2,3,4-tetrahydroisoquinoline

생성물 1

HCID 67721738HCID 67721738, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

(i) To 1.15 g of (R)-(+)-N-acetyl-7,8-dihydroxy-4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline 1/4 hydrate were added 9 ml of 3N hydrochloric acid and 9 ml of ethanol, and the mixture was heated under an argon gas stream for 24 hours. After the reaction solution was cooled, the crystals which separated out were collected by filtration, affording 1.09 g of (R)-(+)-7,8-dihydroxy-4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride monohydrate.

후처리

  1. temperaturethe mixture was heated under an argon gas stream for 24 hours
  2. temperatureAfter the reaction solution was cooled
  3. customthe crystals which separated out
  4. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-7ea080331a9f4b34b887931f635af00e
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05623074

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