Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester

Base Information

Chemical Name:Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester
CAS No.:93604-45-6
Molecular Formula:C₂₄H₂₄N₄O₇S
Molecular Weight:512.543
Hs Code.:

Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester

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Technology Process of Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester

There total 2 articles about Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester 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: 13.4%

: 541-41-3
chloroformic acid ethyl ester

: 93644-77-0
Thiobenzoic acid S-((1R,2S)-2,7-diamino-9-carbamoyloxymethyl-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester

: 93604-45-6
Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester

Guidance literature:: With triethylamine; In tetrahydrofuran; for 4h; Ambient temperature;
DOI:10.1021/jo00203a002

Reference yield:

: 50-07-7
mitomycin C

: 93604-45-6
Thiobenzoic acid S-((1R,2S)-7-amino-9-carbamoyloxymethyl-2-ethoxycarbonylamino-6-methyl-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl) ester

Guidance literature:: Multi-step reaction with 2 steps

1: 13 percent / Na₂S₂O₄, O₂ / H₂O / 0.17 h / Ambient temperature; ph 6

2: 13.4 percent / Et₃N / tetrahydrofuran / 4 h / Ambient temperature

With sodium dithionite; oxygen; triethylamine; In tetrahydrofuran; water;
DOI:10.1021/jo00203a002