(S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:(S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline
CAS No.:548459-37-6
Molecular Formula:C₂₅H₂₄N₂O₃
Molecular Weight:400.477
Hs Code.:

Synonyms:(S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

Suppliers and Price of (S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

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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 (S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

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Technology Process of (S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

There total 3 articles about (S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline 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: 55.0%

: 596087-07-9
1-(2-[(R)-O-acetylmandelyl]aminophenyl)-3,4-dihydroisoquinoline

: 548459-37-6
(S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With sodium cyanoborohydride; acetic acid; at 15 ℃; for 5h;

Reference yield:

: 19260-06-1
1-(2-aminophenyl)-3,4-dihydroisoquinoline

: 548459-37-6
(S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / DMAP; DCC / CH₂Cl₂ / 12 h / 15 °C

2: 55 percent / NaBH₃CN; glac. AcOH / 5 h / 15 °C

With dmap; sodium cyanoborohydride; acetic acid; dicyclohexyl-carbodiimide; In dichloromethane;

Reference yield:

: 51019-43-3
(R)-(-)-O-acetylmandelic acid

: 548459-37-6
(S)-1-(2-[(R)-O-acetylmandelyl]aminophenyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / DMAP; DCC / CH₂Cl₂ / 12 h / 15 °C

2: 55 percent / NaBH₃CN; glac. AcOH / 5 h / 15 °C

With dmap; sodium cyanoborohydride; acetic acid; dicyclohexyl-carbodiimide; In dichloromethane;