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HCID 4616003, 화합물 → 2-(2-Furan-2-ylmethyl-3-oxo-2,3-dihydro-1H-isoindol-1-ylsulfanyl)-N-thiazol-2-yl-acetamide

HRID 2078483
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HRID 2078483 반응식
[OH:1]C1C2C(=CC=CC=2)C(=O)N1CC1SC=CC=1.[O:18]=[C:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]([S:28][CH2:29][C:30]([NH:32][C:33]2[S:34][CH:35]=[CH:36][N:37]=2)=[O:31])[N:20]1[CH2:38][C:39]1S[CH:41]=[CH:42][CH:43]=1>>[O:1]1[CH:41]=[CH:42][CH:43]=[C:39]1[CH2:38][N:20]1[C:19](=[O:18])[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]1[S:28][CH2:29][C:30]([NH:32][C:33]1[S:34][CH:35]=[CH:36][N:37]=1)=[O:31]
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참가 물질

3

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HCID 4616003HCID 4616003, 화합물HCID 166597412-(3-Oxo-2-thiophen-2-ylmethyl-2,3-dihydro-1H-isoindol-1-ylsulfanyl)-N-thiazol-2-yl-acetamide

생성물 1

HCID 166599082-(2-Furan-2-ylmethyl-3-oxo-2,3-dihydro-1H-isoindol-1-ylsulfanyl)-N-thiazol-2-yl-acetamide

실험 절차

Compound 32 was prepared using the synthetic sequence in a manner analogous to the method described for the conversion of compound 12 to compound 14 and illustrated in Scheme 1b. 1H NMR (300 MHz, DMSO): δ 11.96 (s, 1H), 7.71 (d, J=8 Hz, 1H), 7.59 (m, 4H), 7.48 (m, 2H), 7.42 (d, J=4 Hz, 1H), 7.19 (d, J=4 Hz, 1H), 5.76 (s, 1H), 4.97 (d, J=16 Hz, 1H), 4.44 (d, J=16 Hz, 1H), 3.09 (d, J=15 Hz, 1H), 2.95 (d, J=15 Hz, 1H). MS: m/z (MH+) 386.

출처 및 근거

ORD 기록
ord-b7e40afa4f7e4ab0b35747298de2f340
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07928246B2

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