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Hydrochloric Acid → HCID 178503566, 화합물

HRID 1626018
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인쇄 미리보기

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HRID 1626018 반응식
[OH:1][C:2]1[C:7]([NH:8][C:9](=[O:17])[C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([CH3:16])[CH:11]=2)=[C:6]([OH:18])[N:5]=[C:4]([SH:19])[N:3]=1.[OH-].[Na+].I[CH3:23].Cl>O.CN1CCCC1=O>[OH:18][C:6]1[C:7]([NH:8][C:9](=[O:17])[C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([CH3:16])[CH:11]=2)=[C:2]([OH:1])[N:3]=[C:4]([S:19][CH3:23])[N:5]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 14798Sodium HydroxideHCID 178425296HCID 178425296, 화합물

생성물 1

HCID 178503566HCID 178503566, 화합물

시약·촉매·용매 2

HCID 962Water용매
HCID 13387
N-methyl-2-pyrrolidone
용매

반응 조건

온도
0 °C

실험 절차

28.6 g of N-(4,6-dihydroxy-2-mercapto-pyrimidin-5-yl)-3-methyl-benzamide in 280 ml of water were cooled to 0° C. With cooling, 10.3 g of sodium hydroxide were added, and the mixture was stirred at 0° C. for 30 min. Then a solution of 6.4 ml of iodomethane in 108 ml of N-methylpyrrolidin-2-one was added. After completion of the reaction (6 h), the mixture was acidified with 6 N hydrochloric acid, and the precipitate filtered off and dried. 21.3 g of the title compound were obtained.

후처리

  1. temperatureWith cooling
  2. customAfter completion of the reaction (6 h)
  3. filtrationthe precipitate filtered off
  4. customdried

출처 및 근거

ORD 기록
ord-c5b1e2314998471ca23b0360a64de89b
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08785439B2

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