(2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

Base Information

Chemical Name:(2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine
CAS No.:194936-42-0
Molecular Formula:C₃₅H₃₈N₂O₄S
Molecular Weight:582.764
Hs Code.:

Synonyms:(2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

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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 (2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

Chemical Property:

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Technology Process of (2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

There total 3 articles about (2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine 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:

: 2937-50-0
Allyl chloroformate

: 1027584-94-6
(2S,4S)-2-(3-Azido-prop-1-ynyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester

: 194936-42-0
(2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

Guidance literature:: With triethylamine; triphenylphosphine; In tetrahydrofuran; water; at 20 ℃;
DOI:10.7164/antibiotics.50.586

Reference yield:

: 194936-41-9
(2S,4S)-N-t-butoxycarbonyl-2-(3-hydroxy-1-propynyl)-4-tritylthiopyrrolidine

: 194936-42-0
(2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

Guidance literature:: Multi-step reaction with 3 steps

1: NEt₃ / tetrahydrofuran / 0.5 h / 4 °C

2: NaN₃ / dimethylformamide / 1 h / 50 °C

3: PPh₃; NEt₃ / tetrahydrofuran; H₂O / 20 °C

With sodium azide; triethylamine; triphenylphosphine; In tetrahydrofuran; water; N,N-dimethyl-formamide; 1: Substitution / 2: Substitution / 3: Substitution;
DOI:10.7164/antibiotics.50.586

Reference yield:

: 1026929-05-4
(2S,4S)-2-(3-Methanesulfonyloxy-prop-1-ynyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester

: 194936-42-0
(2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1: NaN₃ / dimethylformamide / 1 h / 50 °C

2: PPh₃; NEt₃ / tetrahydrofuran; H₂O / 20 °C

With sodium azide; triethylamine; triphenylphosphine; In tetrahydrofuran; water; N,N-dimethyl-formamide; 1: Substitution / 2: Substitution;
DOI:10.7164/antibiotics.50.586