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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 1787508
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HRID 1787508 반응식
[NH2:1][C:2]1[S:3][C:4]2[CH2:19][C:14]3([O:18][CH2:17][CH2:16][O:15]3)[CH2:13][CH2:12][C:5]=2[C:6]=1[C:7](OCC)=[O:8].C([O-])=O.[NH4+].[CH:24]([NH2:26])=O>>[O:15]1[CH2:16][CH2:17][O:18][C:14]21[CH2:13][CH2:12][C:5]1[C:6]3[C:7](=[O:8])[NH:26][CH:24]=[N:1][C:2]=3[S:3][C:4]=1[CH2:19]2
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참가 물질

4

반응물 3

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 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) in formamide (225 mL) was added ammonium formate (17.8 g, 0.282 mol). The resulting mixture was stirred with 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 was 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. washwas washed with water (2×60 mL), and suction
  7. customdried overnight

출처 및 근거

ORD 기록
ord-ee3cfada88424eb294800670d1a74bec
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07511048B2

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