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Hydrochloric Acid → 2-Propyl-2-(3-thiazol-2-ylureido)pentanoic acid

HRID 612394
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반응식

HRID 612394 반응식
C([O:3][C:4](=[O:21])[C:5]([CH2:18][CH2:19][CH3:20])([NH:9][C:10]([NH:12][C:13]1[S:14][CH:15]=[CH:16][N:17]=1)=[O:11])[CH2:6][CH2:7][CH3:8])C.Cl>[OH-].[Na+]>[CH2:6]([C:5]([NH:9][C:10]([NH:12][C:13]1[S:14][CH:15]=[CH:16][N:17]=1)=[O:11])([CH2:18][CH2:19][CH3:20])[C:4]([OH:21])=[O:3])[CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 110669732-Propyl-2-(3-thiazol-2-ylureido)pentanoic acid ethyl ester

생성물 1

HCID 110873642-Propyl-2-(3-thiazol-2-ylureido)pentanoic acid수율 93%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

10.03 g of the product from stage 4 were dissolved with stirring in 200 ml of semi-concentrated sodium hydroxide solution at a temperature of 20° C. The pH was then adjusted to 4 with concentrated hydrochloric acid and extracted three times with 50 ml portions of dichloromethane. The extracts were washed once with a saturated sodium chloride solution and dried over sodium sulphate. Once the solvent had been removed by distillation, 8.48 g of 2-propyl-2-(3-thiazol-2-ylureido)pentanoic acid (93% of th.) were obtained in the form of white crystals (mp 154-155° C.).

후처리

  1. extractionextracted three times with 50 ml portions of dichloromethane
  2. washThe extracts were washed once with a saturated sodium chloride solution
  3. dry with materialdried over sodium sulphate
  4. customOnce the solvent had been removed by distillation

출처 및 근거

ORD 기록
ord-a0f71aee8cec4cabb861d57f0ea9f4aa
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06004963

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