tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate

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Chemical Name:tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate
CAS No.:214337-20-9
Molecular Formula:C₂₅H₃₃N₃O₆
Molecular Weight:471.554
Hs Code.:

Synonyms:tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate

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Chemical Property of tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate

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Technology Process of tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate

There total 1 articles about tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate 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: 88.5%

: 1148-11-4
N-Benzyloxycarbonyl-L-proline

: tert-butyl (3S,3aR,6aS)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate hydrochloride

: 214337-20-9
tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate

Guidance literature:: N-Benzyloxycarbonyl-L-proline; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1-hydroxybenzotriazol-hydrate; N-ethyl-N,N-diisopropylamine; In acetonitrile; for 0.333333h;

tert-butyl (3S,3aR,6aS)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate hydrochloride; In N,N-dimethyl-formamide; acetonitrile; at 20 ℃; for 24h;
DOI:10.1021/jm030810w

Reference yield: 98.0%

: 214337-20-9
tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate

: 214337-21-0
benzyl (2S)-2-{[(3aS,6S,6aR)-6-methyl-5-oxohexahydropyrrolo[3,2-b]pyrrol-1(2H)-yl]carbonyl}pyrrolidine-1-carboxylate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.75h;
DOI:10.1021/jm030810w

Reference yield:

: 214337-20-9
tert-butyl (3S,3aR,6aS)-4-({(2S)-1-[(benzyloxy)carbonyl]pyrrolidin-2-yl}carbonyl)-3-methyl-2-oxohexahydropyrrolo[3,2-b]pyrrole-1(2H)-carboxylate

: 628725-82-6
tert-butyl (2S)-2-{[(3aS,6S,6aR)-6-methyl-4-(4-nitrophenyl)-5-oxohexahydropyrrolo[3,2-b]pyrrol-1(2H)-yl]carbonyl}pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / TFA / CH₂Cl₂ / 0.75 h / 20 °C

2: 77 percent / H₂ / Pd/C / propan-2-ol; H₂O / 5 h / 20 °C

3: 65 percent / CuCl; K₂CO₃; TDA-1 / p-xylene / Heating

With hydrogen; potassium carbonate; trifluoroacetic acid; copper(l) chloride; palladium on activated charcoal; In dichloromethane; para-xylene; water; isopropyl alcohol;
DOI:10.1021/jm030810w