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Formamide → Spiro[1,3-dioxolane-2,7'-3,5,6,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidine]-4'-one

HRID 1292969
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HRID 1292969 반응식
[CH:1]([NH2:3])=O.[NH2:4][C:5]1[S:6][C:7]2[CH2:22][C:17]3([O:21][CH2:20][CH2:19][O:18]3)[CH2:16][CH2:15][C:8]=2[C:9]=1[C:10](OCC)=[O:11].C([O-])=O.[NH4+]>>[O:18]1[CH2:19][CH2:20][O:21][C:17]21[CH2:16][CH2:15][C:8]1[C:9]3[C:10](=[O:11])[NH:3][CH:1]=[N:4][C:5]=3[S:6][C:7]=1[CH2:22]2
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참가 물질

4

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HCID 713FormamideHCID 2723923Ammonium formateHCID 10902110Ethyl 2-amino-4,7-dihydro-5H-spiro[1-benzothiophere-6,2'-[1,3]dioxolane]-3-carboxylate

생성물 1

HCID 17990151Spiro[1,3-dioxolane-2,7'-3,5,6,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidine]-4'-one수율 88%

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온도
140 °C

실험 절차

To a stirring 225 mL formamide solution of ethyl 2-amino-4,7-dihydro-5H-spiro[1-benzothiophene-6,2′-[1,3]dioxolane]-3-carboxylate (40.0 g, 0.142 mol) was added ammonium formate (17.8 g, 0.282 mol). The contents were stirred with heating at 140° C. for 16 h, after which time the heterogeneous contents were removed from heating, and allowed to cool to rt. The contents were filtered, the solid filter cake washed with water (2×60 mL), and suction dried overnight to afford the desired product as an off-white solid (33.0 g, 88%). 1H-NMR (DMSO-d6) δ 12.35 (broad s, 1H), 8.00 (s, 1H), 3.92 (s, 4H), 2.95 (t, 2H), 2.91 (s, 2H), 1.83 (t, 2H); LCMS RT=1.87 min; [M+H]+=265.2.

후처리

  1. customafter which time the heterogeneous contents were removed
  2. temperaturefrom heating
  3. temperatureto cool to rt
  4. filtrationThe contents were filtered
  5. filtrationthe solid filter cake
  6. washwashed with water (2×60 mL), and suction
  7. customdried overnight

출처 및 근거

ORD 기록
ord-732d866cf5fd486c8a857679e52e9c55
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07238701B2

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