Butyl 4-aminobenzoate → 4-[3-(Naphthalene-2-carbonyl)-thioureido]-benzoic acid butyl ester

HRID 1453817

반응식

HRID 1453817 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11](Cl)=[O:12].[S-:14][C:15]#[N:16].[NH4+].[NH2:18][C:19]1[CH:31]=[CH:30][C:22]([C:23]([O:25][CH2:26][CH2:27][CH2:28][CH3:29])=[O:24])=[CH:21][CH:20]=1>CC(C)=O>[CH2:26]([O:25][C:23](=[O:24])[C:22]1[CH:21]=[CH:20][C:19]([NH:18][C:15]([NH:16][C:11]([C:2]2[CH:3]=[CH:4][C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH:1]=2)=[O:12])=[S:14])=[CH:31][CH:30]=1)[CH2:27][CH2:28][CH3:29]

참가 물질

5

반응물 3

HCID 2482Butyl 4-aminobenzoateHCID 15666Ammonium thiocyanateHCID 752462-Naphthoyl chloride

생성물 1

HCID 103412944-[3-(Naphthalene-2-carbonyl)-thioureido]-benzoic acid butyl ester

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

2-Naphthoyl chloride (190 mg, 1 mmol) is added to a solution of ammonium thiocyanate (200 mg, about 3 mmol) in acetone (5 ml) and stirred at room temperature for 1 hour. Butyl 4-aminobenzoate (180 mg, 0.93 mmol) is added to the reaction mixture. Stirring is continued overnight at room temperature. The solid, which forms is filtered and washed with water (2×5 ml) followed by acetone/hexane (3:1)(2×10 ml) and dried.

후처리

  1. stirringStirring
  2. waitis continued overnight at room temperature
  3. filtrationThe solid, which forms is filtered
  4. washwashed with water (2×5 ml)
  5. customdried

출처 및 근거

ORD 기록
ord-24f3c18a74e549d1a1dadf374496efc3
출처 데이터셋
uspto-grants-2009_01
특허 번호
US07476686B2

연결된 노트

불러오는 중…