2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

Base Information

Chemical Name:2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine
CAS No.:252684-68-7
Molecular Formula:C₁₆H₂₁N₃O₃S
Molecular Weight:335.427
Hs Code.:

Synonyms:2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

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Chemical Property of 2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

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Technology Process of 2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

There total 6 articles about 2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine 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:

: 221658-91-9
N-2-<(2-amino-4-thiazolyl)ethyl>-3,4,5-trimethoxyphenylacetamide

: 252684-68-7
2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: POCl₃ / acetonitrile / 5 h / Heating

2: NaBH₄ / methanol / Ambient temperature

With sodium tetrahydroborate; trichlorophosphate; In methanol; acetonitrile;
DOI:10.1021/jm990012z

Reference yield:

: 4-(3,4,5-trimethoxy-benzyl)-6,7-dihydro-thiazolo[5,4-c]pyridin-2-ylamine

: 252684-68-7
2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

Guidance literature:: With sodium tetrahydroborate; In methanol; Ambient temperature;
DOI:10.1021/jm990012z

Reference yield:

: 951-82-6
3,4,5-trimethoxyphenyl acetic acid

: 252684-68-7
2-amino-4-(3',4',5'-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / oxalyl chloride / benzene / a) RT, 1 h, b) reflux, 2.5 h

2: 71 percent / NaOH / CHCl₃ / 1.5 h / Ambient temperature

3: POCl₃ / acetonitrile / 5 h / Heating

4: NaBH₄ / methanol / Ambient temperature

With sodium hydroxide; sodium tetrahydroborate; oxalyl dichloride; trichlorophosphate; In methanol; chloroform; acetonitrile; benzene;
DOI:10.1021/jm990012z