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Hydrochloric Acid → HCID 9350311, 화합물

HRID 2066945
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인쇄 미리보기

반응식

HRID 2066945 반응식
[CH3:1][C:2]1[C:10]2[C:9](=[O:11])[NH:8][C:7]([CH2:12][N:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)=[N:6][C:5]=2[S:4][C:3]=1[C:19]([O:21]CC)=[O:20].Cl>[OH-].[Na+]>[CH3:1][C:2]1[C:10]2[C:9](=[O:11])[NH:8][C:7]([CH2:12][N:13]3[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]3)=[N:6][C:5]=2[S:4][C:3]=1[C:19]([OH:21])=[O:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 3301642HCID 3301642, 화합물

생성물 1

HCID 9350311HCID 9350311, 화합물수율 92%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

반응 조건

온도
80 °C

실험 절차

671 Milligrams of ethyl 5-methyl-4-oxo-2-piperidinomethyl-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylate was suspended in 8 mL of 0.5N sodium hydroxide, stirred at 80° C. for 2 hours, and allowed to cool off. The reaction liquid was neutralized with 2N hydrochloric acid, and the precipitate was recovered by filtration and dried, to provide 565 mg (92%) of the title compound.

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후처리

  1. temperatureto cool off
  2. customThe reaction liquid
  3. filtrationthe precipitate was recovered by filtration
  4. customdried

출처 및 근거

ORD 기록
ord-3dce37557b6449b8bb14e277307fcf44
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08293754B2

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