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Hydroxide → 2-[(1-Benzothien-3-ylcarbonyl)amino]-4-chlorobenzoic acid

HRID 555928
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HRID 555928 반응식
[NH2:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:3]=1[C:4]([O:6]C)=[O:5].CCN(C(C)C)C(C)C.[S:22]1[CH:26]=[C:25]([C:27](O)=[O:28])[C:24]2[CH:30]=[CH:31][CH:32]=[CH:33][C:23]1=2.O=P(Cl)(Cl)Cl.NCCNCCN.CCN(C(C1C=CC=C(C)C=1)=O)CC.[OH-]>ClCCCl.CC(N(C)C)=O>[S:22]1[C:23]2[CH:33]=[CH:32][CH:31]=[CH:30][C:24]=2[C:25]([C:27]([NH:1][C:2]2[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:3]=2[C:4]([OH:6])=[O:5])=[O:28])=[CH:26]1
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참가 물질

10

반응물 7

HCID 961HydroxideHCID 4284N,N-diethyl-m-toluamideHCID 8111DiethylenetriamineHCID 24813Phosphorus oxychlorideHCID 80001Methyl 4-chloroanthranilateHCID 81531DiisopropylethylamineHCID 601280Benzo(b)thiophene-3-carboxylic acid

생성물 1

HCID 161234902-[(1-Benzothien-3-ylcarbonyl)amino]-4-chlorobenzoic acid

시약·촉매·용매 2

HCID 111,2-Dichloroethane용매2회HCID 31374Dimethylacetamide용매

실험 절차

In a 2 mL vial, methyl 2-amino-4-chlorobenzoate (7.4 mg, 40 μmol) was dissolved into a mixture of 655 μL DCE and 120 μL DMA, followed by addition of DIPEA (600 μmol, 15 eq.). Benzo[b]thiophene-3-carboxylic acid (21.4 mg, 120 μmol, 3 eq.) and POCl3 (18.2 mg, 120 μmol, 3 eq.) were added. The reaction mixture was capped and stirred at room temperature overnight. Another 700 μL of DCE was added to the reaction mixture along with the following resin bound reagents: a resin bound diethylene triamine (PL-DETA, Polymer Labs, 297 μmol, 7.4 eq.) and a hydroxide ion exchange resin (PL-MP Hydroxide, Polymer Labs, 800 μmol, 20 eq.). The vial was recapped and shaken at room temperature overnight. The resin in the reaction mixture was filtered off, rinsed with 300 μL of MeOH and discarded. The combined filtrates were concentrated down in vacuo. The residue was re-dissolved into 1 mL of DMA and 280 μL of 1M aqueous NaOH. The solution was stirred at room temperature overnight. The desired product was isolated directly from this solution via reverse phase C18 preparative HPLC (water/acetonitrile w/0.1% formic acid, 30%-100% eluant gradient) to yield the final product (2.9 mg, 95% purity). MS (EI) for C16H10ClNO3S: 332 (M+H).

후처리

  1. customThe reaction mixture was capped
  2. stirringshaken at room temperature overnight
  3. filtrationThe resin in the reaction mixture was filtered off
  4. washrinsed with 300 μL of MeOH
  5. concentrationThe combined filtrates were concentrated down in vacuo
  6. dissolutionThe residue was re-dissolved into 1 mL of DMA and 280 μL of 1M aqueous NaOH
  7. stirringThe solution was stirred at room temperature overnight

출처 및 근거

ORD 기록
ord-4c60364aaf524e57b294bb048097d471
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08053454B2

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