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Succinic anhydride → 3-[3-(3-Tert-butyloxycarbonylaminophenyl)-1,2,4-oxadiazol-5-yl]propionic acid

HRID 584122
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반응식

HRID 584122 반응식
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH2:3][CH2:2]1.[C:8]([O:12][C:13](=[O:25])[NH:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([C:21](=[NH:24])[NH:22]O)[CH:16]=1)([CH3:11])([CH3:10])[CH3:9]>CN(C=O)C>[C:8]([O:12][C:13]([NH:14][C:15]1[CH:16]=[C:17]([C:21]2[N:24]=[C:4]([CH2:3][CH2:2][C:1]([OH:6])=[O:7])[O:5][N:22]=2)[CH:18]=[CH:19][CH:20]=1)=[O:25])([CH3:11])([CH3:9])[CH3:10]
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참가 물질

4

반응물 2

HCID 7922Succinic anhydrideHCID 178452725HCID 178452725, 화합물

생성물 1

HCID 223431013-[3-(3-Tert-butyloxycarbonylaminophenyl)-1,2,4-oxadiazol-5-yl]propionic acid

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
120 °C

실험 절차

Succinic anhydride (14 mg, 0.14 mmol) and [3-(N-hydroxycarbamimidoyl)-phenyl]-carbamic acid tert-butyl ester (35 mg, 0.14 mmol) were dissolved in 0.25 mL DMF and heated at 120° C. for 2 h. The cooled solution was evaporated and dried to yield 3-[3-(3-tert-butoxycarbonylamino-phenyl)-[1,2,4]oxadiazol-5-yl]-propionic acid which was used without further purification.

후처리

  1. customThe cooled solution was evaporated
  2. customdried

출처 및 근거

ORD 기록
ord-45f2726504e34f3b8de66244cb47619b
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06924284B2

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