2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole

Base Information

Chemical Name:2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole
CAS No.:135430-44-3
Molecular Formula:C₁₉H₁₇N₅O₂S₂
Molecular Weight:411.508
Hs Code.:

Synonyms:2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole

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Chemical Property of 2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole

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Technology Process of 2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole

There total 4 articles about 2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 33.0%

: 135430-60-3
2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)thio>-1H-benzimidazole

: 135430-44-3
2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In chloroform; at 15 ℃; for 0.5h;
DOI:10.1016/0223-5234(91)90024-H

Reference yield:

: 135429-75-3
4-((benzyloxycarbonyl)glycyl)amino-5-hydroxymethyl-3-phenylisothiazole

: 135430-44-3
2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole

Guidance literature:: Multi-step reaction with 3 steps

1: 75.5 percent / n-Bu₃P, pyridine / Ambient temperature

2: 98.9 percent / 25percent HBr-AcOH / 1.5 h / Ambient temperature

3: 33 percent / m-chloroperbenzoic acid / CHCl₃ / 0.5 h / 15 °C

With pyridine; tributylphosphine; hydrogen bromide; acetic acid; 3-chloro-benzenecarboperoxoic acid; In chloroform;
DOI:10.1016/0223-5234(91)90024-H

Reference yield:

: 135429-77-5
4-<(benzyloxycarbonyl)glycyl>amino-5-ethoxycarbonyl-3-phenylisothiazole

: 135430-44-3
2-<((4-glycylamino-3-phenylisothiazol-5-yl)methyl)sulfinyl>-1H-benzimidazole

Guidance literature:: Multi-step reaction with 4 steps

1: 62.9 percent / LiBH₄ / tetrahydrofuran / 3 h / Ambient temperature

2: 75.5 percent / n-Bu₃P, pyridine / Ambient temperature

3: 98.9 percent / 25percent HBr-AcOH / 1.5 h / Ambient temperature

4: 33 percent / m-chloroperbenzoic acid / CHCl₃ / 0.5 h / 15 °C

With pyridine; lithium borohydride; tributylphosphine; hydrogen bromide; acetic acid; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; chloroform;
DOI:10.1016/0223-5234(91)90024-H