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Hydrochloric Acid → HCID 178526038, 화합물

HRID 1045096
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HRID 1045096 반응식
Br[CH2:2][C:3]([OH:5])=[O:4].[Cl:6][C:7]1[C:16]([C:17]#[C:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:15][C:10]2[NH:11][C:12](=[S:14])[NH:13][C:9]=2[CH:8]=1.[OH-].[K+].Cl>CCO.O>[Cl:6][C:7]1[C:16]([C:17]#[C:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:15][C:10]2[N:11]=[C:12]([S:14][CH2:2][C:3]([OH:5])=[O:4])[NH:13][C:9]=2[CH:8]=1
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 6227Bromoacetic AcidHCID 14797Potassium HydroxideHCID 86762102HCID 86762102, 화합물

생성물 1

HCID 178526038HCID 178526038, 화합물

시약·촉매·용매 2

HCID 702Ethanol용매2회
HCID 962
Water
용매

실험 절차

A solution of bromoacetic acid (47.8 mg, 0.344 mmol) in EtOH (1 mL) was added dropwise to a 20 mL scintillation vial equipped with a stirring bar and a septum cap containing a solution of compound 1-3 (49.0 mg, 0.172 mmol) in EtOH (1 mL). To this solution, 1M KOH (2 mL) was added dropwise, and the resulting mixture was stirred at rt for 1 h. The reaction mixture was then diluted with water (4 mL) and acidified with 10% aqueous HCl. The solution was extracted with EtOAc (3 mL then twice 1 mL), extracts were combined and evaporated to dryness in vacuo. The resulting oily residue was dissolved in DMSO (1.0 mL), filtered and purified by reverse-phase HPLC to give the title compound as white solid. LR-MS (API-ES): calculated for C17H11ClN2O2S 342.0, observed m/e 343.1 (M+H)+ (Rt 7.71 min).

후처리

  1. customvial equipped with a stirring bar
  2. customa septum cap
  3. extractionThe solution was extracted with EtOAc (3 mL
  4. customevaporated to dryness in vacuo
  5. dissolutionThe resulting oily residue was dissolved in DMSO (1.0 mL)
  6. filtrationfiltered
  7. custompurified by reverse-phase HPLC

출처 및 근거

ORD 기록
ord-a0a4f4a854834a28923d43e04c0bf4ca
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08563746B2

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