3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide

Base Information

Chemical Name:3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide
CAS No.:1202755-95-0
Molecular Formula:C₂₂H₂₃ClN₆O₃S
Molecular Weight:486.982
Hs Code.:

Synonyms:3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide

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Chemical Property of 3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide

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Technology Process of 3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide

There total 6 articles about 3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide 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: 16.0%

: 1202759-69-0
C₂₀H₂₂N₆O₂S

: 79-04-9
chloroacetyl chloride

: 1202755-95-0
3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide

Guidance literature:: With triethylamine; In 1-methyl-pyrrolidin-2-one; at 0 - 20 ℃;

Reference yield:

: 164148-92-9
tert-butyl 6-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1202755-95-0
3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / butan-1-ol / 0.75 h / 120 °C / Microwave irradiation

2: hydrogenchloride / water / 12 h / 100 °C

3: triethylamine / 1-methyl-pyrrolidin-2-one / 0 - 20 °C

With triethylamine; N-ethyl-N,N-diisopropylamine; hydrogenchloride; In 1-methyl-pyrrolidin-2-one; water; butan-1-ol;

Reference yield:

: 1154424-63-1
tert-butyl 6-benzyloxycarbonylamino-3,4-dihydro-1H-isoquinoline-2-carboxylate

: 1202755-95-0
3-(4-(2-(2-chloroacetyl)-1,2,3,4-tetrahydroisoquinolin-6-ylamino)-5-methylpyrimidin-2-ylamino)benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium formate / palladium(II) hydroxide / ethanol / 6 h / Reflux

2: N-ethyl-N,N-diisopropylamine / butan-1-ol / 0.75 h / 120 °C / Microwave irradiation

3: hydrogenchloride / water / 12 h / 100 °C

4: triethylamine / 1-methyl-pyrrolidin-2-one / 0 - 20 °C

With ammonium formate; triethylamine; N-ethyl-N,N-diisopropylamine; hydrogenchloride; palladium(II) hydroxide; In 1-methyl-pyrrolidin-2-one; ethanol; water; butan-1-ol;