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tert-butyl N-[4-[[[(6S)-3-(naphthalen-1-ylsulfonylamino)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamate → Naphthalenesulfonamide

HRID 10994
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HRID 10994 반응식
C(OC(=O)NC(=N)C1C=CC(CNC([C@H]2N3C(=O)C(NS(C)(=O)=O)=CN=C3CC2)=O)=CC=1)(C)(C)C.C(OC(=O)NC(C1C=CC(CNC([C@H]2N3C(=O)C(N(CC)CC)=CN=C3CC2)=O)=CC=1)=N)(C)(C)C.C(OC(=O)NC(=N)C1C=CC(CNC([C@H]2N3C(=O)C([NH:98][S:99]([C:102]4[C:111]5[C:106](=[CH:107][CH:108]=[CH:109][CH:110]=5)[CH:105]=[CH:104][CH:103]=4)(=[O:101])=[O:100])=CN=C3CC2)=O)=CC=1)(C)(C)C>>[C:102]1([S:99]([NH2:98])(=[O:100])=[O:101])[C:111]2[C:106](=[CH:107][CH:108]=[CH:109][CH:110]=2)[CH:105]=[CH:104][CH:103]=1
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참가 물질

4

반응물 3

HCID 145857221tert-butyl N-[4-[[[(6S)-3-(naphthalen-1-ylsulfonylamino)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamateHCID 145857232tert-butyl N-[4-[[[(6S)-3-(methanesulfonamido)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamateHCID 145857233tert-butyl N-[4-[[[(6S)-3-(diethylamino)-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carbonyl]amino]methyl]benzenecarboximidoyl]carbamate

생성물 1

HCID 163571
Naphthalenesulfonamide
수율 30%

실험 절차

Following a procedure similar to that for the preparation of 16a, intermediate 3a (50 mg, 0.117 mmol) and 1-napthylene sulfonyl chloride (39.8 mg, 0.176 mmol) yielded 21.7 mg (30.0%) of 1-napthalene sulfonamide intermediate 30a. MS (ESI) 617.0 (M+H+).

출처 및 근거

ORD 기록
ord-52e7df54d8284410b978de744febdd8b
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07094783B2

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