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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → tert-Butyl 3-thioureidopropylcarbamate

HRID 1755461
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반응식

HRID 1755461 반응식
C([NH:9][C:10](=[S:23])[NH:11][CH2:12][CH2:13][CH2:14][NH:15][C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19])(=O)C1C=CC=CC=1.[OH-].[Na+]>CO>[NH:11]([CH2:12][CH2:13][CH2:14][NH:15][C:16](=[O:22])[O:17][C:18]([CH3:20])([CH3:19])[CH3:21])[C:10]([NH2:9])=[S:23]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 14280415tert-Butyl 3-(3-benzoylthioureido)propylcarbamate

생성물 1

HCID 20616909tert-Butyl 3-thioureidopropylcarbamate수율 72%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of material from Example 58 (6.89 g, 20.43 mmol) in MeOH (40 mL) is slowly added aqueous 5M NaOH (4.49 mL, 22.47 mmol) and the reaction is allowed to stir for 1 h at room temp. The solvent is removed in vacuo, the residue is neutralized with acetic acid and partitioned between water and EtOAc. The water layer is extracted with EtOAC, the organic layers are combined, washed with brine, dried over Na2SO4, filtered and evaporated to dryness to give 3.43 g (50.2%) of the title compound. LC/MS (Condition A): ret. T=2.54 min, (M+Na) 256.13.

후처리

  1. customThe solvent is removed in vacuo
  2. custompartitioned between water and EtOAc
  3. extractionThe water layer is extracted with EtOAC
  4. washwashed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-afabd929efe7455c8ee92fb226c440aa
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09169295B2

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